| Year | Citation | Score | |||
|---|---|---|---|---|---|
| 2020 | Fekete G, Kovács G, Garami M. Dr. Dezső Schuler (1927–2020) Orvosi Hetilap. 161: 1972-1973. PMID 33190129 DOI: 10.1556/650.2020.HO2673 | 0.47 | |||
| 2020 | Eggermann T, Brück J, Knopp C, Fekete G, Kratz C, Tasic V, Kurth I, Elbracht M, Eggermann K, Begemann M. Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important. Journal of Molecular Medicine (Berlin, Germany). PMID 32839827 DOI: 10.1007/S00109-020-01966-Z | 0.335 | |||
| 2020 | Lengyel A, Pinti É, Pikó H, Jávorszky E, David D, Tihanyi M, Gönczi É, Kiss E, Tóth Z, Tory K, Fekete G, Haltrich I. Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature. European Journal of Medical Genetics. 104027. PMID 32758661 DOI: 10.1016/J.Ejmg.2020.104027 | 0.332 | |||
| 2020 | Eßinger C, Karch S, Moog U, Fekete G, Lengyel A, Pinti E, Eggermann T, Begemann M. Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome. Clinical Epigenetics. 12: 63. PMID 32393365 DOI: 10.1186/S13148-020-00856-Y | 0.31 | |||
| 2019 | Madar L, Szakszon K, Pfliegler G, Szabó GP, Brúgós B, Ronen N, Papp J, Zahuczky K, Szakos E, Fekete G, Oláh É, Koczok K, Balogh I. FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies. Journal of Biotechnology. PMID 31163209 DOI: 10.1016/J.Jbiotec.2019.05.012 | 0.376 | |||
| 2018 | Lengyel A, Kosik A, Pinti É, Lódi C, Tory K, Fekete G, Haltrich I. [Trisomy 9p and clinical heterogeneity: case report of an unusual presentation]. Orvosi Hetilap. 159: 1994-2000. PMID 30474384 DOI: 10.1556/650.2018.31223 | 0.302 | |||
| 2018 | Beke A, Piko H, Haltrich I, Karcagi V, Rigo J, Molnar MJ, Fekete G. Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations. Bmc Medical Genetics. 19: 113. PMID 29986653 DOI: 10.1186/S12881-018-0634-5 | 0.323 | |||
| 2018 | Doleschall M, Török D, Mészáros K, Luczay A, Halász Z, Németh K, Szücs N, Kiss R, Tőke J, Sólyom J, Fekete G, Patócs A, Igaz P, Tóth M. [Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia]. Orvosi Hetilap. 159: 269-277. PMID 29429350 DOI: 10.1556/650.2018.30986 | 0.358 | |||
| 2018 | Ács OD, Péterfia B, Hollósi P, Haltrich I, Sallai Á, Luczay A, Buiting K, Horsthemke B, Török D, Szabó A, Fekete G. [Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome]. Orvosi Hetilap. 159: 64-69. PMID 29307221 DOI: 10.1556/650.2018.30918 | 0.31 | |||
| 2017 | Miklós G, Fekete G, Haltrich I, Tóth M, Reismann P. [Williams-Beuren syndrome (Williams syndrome). Case report]. Orvosi Hetilap. 158: 1883-1888. PMID 29153020 DOI: 10.1556/650.2017.30905 | 0.334 | |||
| 2017 | Meyer R, Soellner L, Begemann M, Dicks S, Fekete G, Rahner N, Zerres K, Elbracht M, Eggermann T. Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management. The Journal of Pediatrics. PMID 28529015 DOI: 10.1016/J.Jpeds.2017.04.018 | 0.336 | |||
| 2017 | Medvecz M, Fekete G, Mayer B, Kárpáti S. 235 Genotype-phenotype correlation in vascular Ehlers-Danlos syndrome: Novel duplication mutation of COL3A1 gene in a large pedigree Journal of Investigative Dermatology. 137. DOI: 10.1016/J.Jid.2017.07.232 | 0.323 | |||
| 2016 | Sachwitz J, Meyer R, Fekete G, Spranger S, Matulevičienė A, Kučinskas V, Bach A, Luczay A, Ortiz Brüchle N, Eggermann K, Zerres K, Elbracht M, Eggermann T. NSD1 duplication in Silver-Russell syndrome (SRS): Molecular karyotyping in patients with SRS features. Clinical Genetics. PMID 27172843 DOI: 10.1111/Cge.12803 | 0.355 | |||
| 2016 | Sachwitz J, Strobl-Wildemann G, Fekete G, Ambrozaitytė L, Kučinskas V, Soellner L, Begemann M, Eggermann T. Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. Bmc Medical Genetics. 17: 20. PMID 26969265 DOI: 10.1186/S12881-016-0280-8 | 0.346 | |||
| 2016 | Odler B, Cseh Á, Constantin T, Fekete G, Losonczy G, Tamási L, Benke K, Szilveszter B, Müller V. Long time enzyme replacement therapy stabilizes obstructive lung disease and alters peripheral immune cell subsets in Fabry patients. The Clinical Respiratory Journal. PMID 26763180 DOI: 10.1111/Crj.12446 | 0.305 | |||
| 2014 | Haltrich I, Pikó H, Kiss E, Tóth Z, Karcagi V, Fekete G. A de novo atypical ring sSMC(22) characterized by array CGH in a boy with cat-eye syndrome. Molecular Cytogenetics. 7: 37. PMID 24959203 DOI: 10.1186/1755-8166-7-37 | 0.3 | |||
| 2014 | Balla B, Árvai K, Horváth P, Tobiás B, Takács I, Nagy Z, Dank M, Fekete G, Kósa JP, Lakatos P. Fast and robust next-generation sequencing technique using ion torrent personal genome machine for the screening of neurofibromatosis type 1 (NF1) gene. Journal of Molecular Neuroscience : Mn. 53: 204-10. PMID 24676943 DOI: 10.1007/S12031-014-0286-7 | 0.304 | |||
| 2014 | Pállinger E, Erdélyi D, Kovács G, Kriván G, Korponay Z, Fekete G, Szabó A, Falus A, Dérfalvi B. [Flow cytometry in the diagnosis of hemophagocytic lymphohistiocytosis in a case with fatal outcome]. Orvosi Hetilap. 155: 389-95. PMID 24583560 DOI: 10.1556/Oh.2014.29790 | 0.301 | |||
| 2013 | Beke A, Piko H, Haltrich I, Csomor J, Matolcsy A, Fekete G, Rigo J, Karcagi V. Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure. Molecular Cytogenetics. 6: 62. PMID 24359613 DOI: 10.1186/1755-8166-6-62 | 0.31 | |||
| 2013 | Patócs B, Németh K, Garami M, Arató G, Kovalszky I, Szendrői M, Fekete G. Multiple splice variants of EWSR1-ETS fusion transcripts co-existing in the Ewing sarcoma family of tumors. Cellular Oncology (Dordrecht). 36: 191-200. PMID 23494411 DOI: 10.1007/S13402-013-0126-8 | 0.56 | |||
| 2013 | Chilian B, Abdollahpour H, Bierhals T, Haltrich I, Fekete G, Nagel I, Rosenberger G, Kutsche K. Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci. Clinical Genetics. 84: 560-5. PMID 23350639 DOI: 10.1111/Cge.12105 | 0.353 | |||
| 2013 | Haltrich I, Csóka M, Kovács G, Török D, Alpár D, Ottoffy G, Fekete G. Six cases of rare gene amplifications and multiple copy of fusion gene in childhood acute lymphoblastic leukemia. Pathology Oncology Research : Por. 19: 123-8. PMID 22528566 DOI: 10.1007/S12253-012-9533-9 | 0.327 | |||
| 2012 | Patócs B, Németh K, Garami M, Arató G, Kovalszky I, Szendroi M, Fekete G. Utilisation of fluorescent multiplex PCR and laser-induced capillary electrophoresis for the diagnosis of Ewing family of tumours in formalin-fixed paraffin-embedded tissues. Journal of Clinical Pathology. 65: 1112-8. PMID 23015660 DOI: 10.1136/Jclinpath-2012-201154 | 0.559 | |||
| 2010 | Constantin T, Székely A, Ponyi A, Gulácsy V, Ambrus C, Kádár K, Vastagh I, Dajnoki A, Tóth B, Bokrétás G, Müller V, Katona M, Medvecz M, Fiedler O, Széchey R, ... ... Fekete G, et al. Management of Fabry disease | Fabry-betegség - Terápiás útmutató Orvosi Hetilap. 151: 1243-1251. PMID 20656661 DOI: 10.1556/Oh.2010.28796 | 0.596 | |||
| 2010 | Milánkovics I, Németh K, Somogyi C, Schuler A, Fekete G. High frequencies of biotinidase (BTD) gene mutations in the Hungarian population. Journal of Inherited Metabolic Disease. 33: S289-92. PMID 20549359 DOI: 10.1007/S10545-010-9152-0 | 0.33 | |||
| 2010 | Milánkovics I, Schuler A, Kámory E, Csókay B, Fodor F, Somogyi C, Németh K, Fekete G. Molecular and clinical analysis of patients with classic and Duarte galactosemia in western Hungary. Wiener Klinische Wochenschrift. 122: 95-102. PMID 20213376 DOI: 10.1007/S00508-010-1311-7 | 0.311 | |||
| 2010 | Constantin T, Rákóczi E, Ponyi A, Ambrus C, Kádár K, Vastagh I, Dajnoki A, Tóth B, Bokrétás G, Müller V, Katona M, Csikós M, Fiedler O, Széchey R, Varga E, ... ... Fekete G, et al. Fabry disease diagnostic guideline | Fabry-betegség: Diagnosztikai útmutató Orvosi Hetilap. 151: 243-249. PMID 20133243 DOI: 10.1556/Oh.2010.28795 | 0.595 | |||
| 2010 | Sallai A, Sólyom J, Dobos M, Szabó J, Halász Z, Ságodi L, Niederland T, Kozári A, Bertalan R, Ugocsai P, Fekete G. Y-chromosome markers in Turner syndrome: Screening of 130 patients. Journal of Endocrinological Investigation. 33: 222-7. PMID 19625757 DOI: 10.1007/Bf03345783 | 0.322 | |||
| 2009 | Milánkovics I, Schuler A, Németh K, Somogyi C, Fekete G. [Frequencies of the Los Angeles and Duarte galactose-1-phosphate uridyltransferase variant alleles in the Hungarian population]. Orvosi Hetilap. 150: 1301-5. PMID 19581158 DOI: 10.1556/Oh.2009.28671 | 0.301 | |||
| 2009 | Hauser P, Hanzély Z, Máthé D, Szabó E, Barna G, Sebestyén A, Jeney A, Schuler D, Fekete G, Garami M. Effect of somatostatin analogue octreotide in medulloblastoma in xenograft and cell culture study. Pediatric Hematology and Oncology. 26: 363-74. PMID 19579083 DOI: 10.1080/08880010902973293 | 0.538 | |||
| 2009 | Constantin T, Kálovics T, Ponyi A, Nagy E, Sallai K, Szabó L, Garami M, Müller J, Gergely P, Dankó K, Fekete G, Kálmánchey R. Prevalence of antiphospholipid and antinuclear antibodies in children with epilepsy. Medical Science Monitor : International Medical Journal of Experimental and Clinical Research. 15: CR164-9. PMID 19333200 | 0.524 | |||
| 2008 | Erdos M, Németh K, Tóth B, Constantin T, Rákóczi E, Ponyi A, Dajnoki A, Grubits J, Pintér I, Garzuly F, Hahn K, Bencsik K, Vécsei L, Fekete G, Maródi L. Novel sequence variants of the alpha-galactosidase A gene in patients with Fabry disease. Molecular Genetics and Metabolism. 95: 224-8. PMID 18849176 DOI: 10.1016/J.Ymgme.2008.09.002 | 0.314 | |||
| 2008 | Haltrich I, Csóka M, Kovács G, Fekete G. [Cytogenetic and FISH findings are complementary in childhood ALL]. Magyar Onkologia. 52: 283-91. PMID 18845499 DOI: 10.1556/Monkol.52.2008.3.6 | 0.316 | |||
| 2008 | Haltrich I, Csóka M, Kovács G, Fekete G. [Intrachromosomal amplification of AML1 gene in childhood acute lymphoblastic leukemia]. Orvosi Hetilap. 149: 1143-6. PMID 18539581 DOI: 10.1556/Oh.2008.28388 | 0.335 | |||
| 2008 | Halász Z, Bertalan R, Toke J, Patócs A, Tóth M, Fekete G, Gláz E, Rácz K. Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency. Journal of Endocrinological Investigation. 31: 74-8. PMID 18296909 DOI: 10.1007/Bf03345570 | 0.351 | |||
| 2008 | Sallai A, Hosszú E, Gergics P, Rácz K, Fekete G. Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases. European Journal of Pediatrics. 167: 441-6. PMID 17576593 DOI: 10.1007/S00431-007-0532-X | 0.338 | |||
| 2007 | Constantin T, Ponyi A, Kálovics T, Orbán I, Molnár K, Dérfalvy B, Dicso F, Sallai A, Garami M, Balogh Z, Szalai Z, Fekete G, Dankó K. [Disease course, frequency of relapses and survival of patients with juvenile or adult dermatomyositis]. Orvosi Hetilap. 148: 1989-97. PMID 17932005 DOI: 10.1556/Oh.2007.27907 | 0.571 | |||
| 2006 | Halász Z, Toke J, Patócs A, Bertalan R, Tömböl Z, Sallai A, Hosszú E, Muzsnai A, Kovács L, Sólyom J, Fekete G, Rácz K. High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency. Endocrine. 30: 255-60. PMID 17526936 DOI: 10.1007/S12020-006-0002-7 | 0.367 | |||
| 2006 | Scheiber D, Fekete G, Urban Z, Tarjan I, Balaton G, Kosa L, Nagy K, Vajo Z. Echocardiographic findings in patients with Williams-Beuren syndrome. Wiener Klinische Wochenschrift. 118: 538-42. PMID 17009066 DOI: 10.1007/S00508-006-0658-2 | 0.303 | |||
| 2006 | Laki J, Laki I, Németh K, Ujhelyi R, Bede O, Endreffy E, Bolbás K, Gyurkovits K, Csiszér E, Sólyom E, Dobra G, Halász A, Pozsonyi E, Rajczy K, Prohászka Z, ... Fekete G, et al. The 8.1 ancestral MHC haplotype is associated with delayed onset of colonization in cystic fibrosis. International Immunology. 18: 1585-90. PMID 16987934 DOI: 10.1093/Intimm/Dxl091 | 0.315 | |||
| 2006 | Hauser P, Hanzély Z, Jakab Z, Oláh L, Szabó E, Jeney A, Schuler D, Fekete G, Bognár L, Garami M. Expression and prognostic examination of heat shock proteins (HSP 27, HSP 70, and HSP 90) in medulloblastoma. Journal of Pediatric Hematology/Oncology. 28: 461-6. PMID 16825994 DOI: 10.1097/01.Mph.0000212954.35727.Ad | 0.495 | |||
| 2006 | Constantin T, Ponyi A, Orbán I, Molnár K, Dérfalvi B, Dicso F, Kálovics T, Müller J, Garami M, Sallai A, Balogh Z, Szalai Z, Fekete G, Dankó K. National registry of patients with juvenile idiopathic inflammatory myopathies in Hungary--clinical characteristics and disease course of 44 patients with juvenile dermatomyositis. Autoimmunity. 39: 223-32. PMID 16769656 DOI: 10.1080/08916930600622819 | 0.604 | |||
| 2006 | Kure S, Kato K, Dinopoulos A, Gail C, DeGrauw TJ, Christodoulou J, Bzduch V, Kalmanchey R, Fekete G, Trojovsky A, Plecko B, Breningstall G, Tohyama J, Aoki Y, Matsubara Y. Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia. Human Mutation. 27: 343-52. PMID 16450403 DOI: 10.1002/Humu.20293 | 0.321 | |||
| 2006 | Haltrich I, Kost-Alimova M, Kovács G, Klein G, Fekete G, Imreh S. Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients European Journal of Haematology. 76: 124-133. PMID 16405433 DOI: 10.1111/J.1600-0609.2005.00576.X | 0.309 | |||
| 2006 | Kovacs GT, Muller J, Csoka M, Vonnak E, Erlaky H, Farkas A, Somlai A, Fekete G. Use of Erythropoietin (EPO) in Children with Malignancies. Blood. 108: 5533-5533. DOI: 10.1182/Blood.V108.11.5533.5533 | 0.321 | |||
| 2005 | Müller J, Garami M, Constantin T, Schmidt M, Fekete G, Kovács G. Meropenem in the treatment of febrile neutropenic children. Pediatric Hematology and Oncology. 22: 277-84. PMID 16020114 DOI: 10.1080/08880010590935167 | 0.576 | |||
| 2005 | Horváth J, Fliegauf M, Olbrich H, Kispert A, King SM, Mitchison H, Zariwala MA, Knowles MR, Sudbrak R, Fekete G, Neesen J, Reinhardt R, Omran H. Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients. American Journal of Respiratory Cell and Molecular Biology. 33: 41-7. PMID 15845866 DOI: 10.1165/Rcmb.2004-0335Oc | 0.556 | |||
| 2005 | Ponyi A, Constantin T, Balogh Z, Szalai Z, Borgulya G, Molnár K, Tefner I, Garami M, Fekete G, Dankó K. Disease course, frequency of relapses and survival of 73 patients with juvenile or adult dermatomyositis. Clinical and Experimental Rheumatology. 23: 50-6. PMID 15789887 | 0.535 | |||
| 2004 | Garami M, Schuler D, Babosa M, Borgulya G, Hauser P, Müller J, Paksy A, Szabó E, Hidvégi M, Fekete G. Fermented Wheat Germ Extract Reduces Chemotherapy-Induced Febrile Neutropenia in Pediatric Cancer Patients. Journal of Pediatric Hematology/Oncology. 26: 631-635. PMID 27811603 DOI: 10.1097/01.Mph.0000141897.04996.21 | 0.578 | |||
| 2004 | Garami M, Schuler D, Babosa M, Borgulya G, Hauser P, Müller J, Paksy A, Szabó E, Hidvégi M, Fekete G. Fermented wheat germ extract reduces chemotherapy-induced febrile neutropenia in pediatric cancer patients. Journal of Pediatric Hematology/Oncology. 26: 631-5. PMID 15454833 | 0.542 | |||
| 2004 | Dobos M, Fekete G, Raff R, Schubert R, Szabó J, Halász Z, Lukács V, Eggermann T, Schwanitz G. Ring Chromosome 18: Clinical, Cytogenetic and Molecular Genetic Studies on Four Patients International Journal of Human Genetics. 4: 197-200. DOI: 10.1080/09723757.2004.11885892 | 0.31 | |||
| 2003 | Müller J, Kovács G, Garami M, Schmidt M, Fekete G. [Meropenem therapy in children with febrile neutropenia]. Orvosi Hetilap. 144: 2115-20. PMID 14661443 | 0.534 | |||
| 2003 | Constantin T, Ponyi A, Garami M, Gergely L, Fekete G, Dankó K. [Clinical characteristics of juvenile dermatomyositis]. Orvosi Hetilap. 144: 1245-50. PMID 12901181 | 0.504 | |||
| 2003 | Scheiber D, Barta C, Halász Z, Sallai A, Rácz K, Ságodi L, Fekete G, Hiort O, Sólyom J. Mutational analysis of Hungarian patients with androgen insensitivity syndrome. Journal of Pediatric Endocrinology & Metabolism : Jpem. 16: 367-73. PMID 12705360 DOI: 10.1515/Jpem.2003.16.3.367 | 0.374 | |||
| 2003 | Török D, Halász Z, Garami M, Homoki J, Fekete G, Sólyom J. Limited value of serum steroid measurements in identification of mild form of 21-hydroxylase deficiency. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. 111: 27-32. PMID 12605347 DOI: 10.1055/S-2003-37497 | 0.559 | |||
| 2002 | Kure S, Kojima K, Ichinohe A, Maeda T, Kalmanchey R, Fekete G, Berg SZ, Filiano J, Aoki Y, Suzuki Y, Izumi T, Matsubara Y. Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia. Annals of Neurology. 52: 643-6. PMID 12402263 DOI: 10.1002/Ana.10367 | 0.334 | |||
| 2002 | Endreffy E, Németh K, Fekete G, Gyurkovits K, Stankovics J, Szabó Á, Sólyom E, Dolinay T, Raskó I, László A. Molecular Genetic Diagnostic Difficulties in Two Hungarian Gypsy Samples with Cystic Fibrosis International Journal of Human Genetics. 2: 41-44. DOI: 10.31901/24566330.2002/02.01.08 | 0.321 | |||
| 2001 | Theodoropoulou M, Barta C, Szoke M, Guttman A, Staub M, Niederland T, Sólyom J, Fekete G, Sasvari-Szekely M. Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification. Fetal Diagnosis and Therapy. 16: 237-40. PMID 11399887 DOI: 10.1159/000053918 | 0.304 | |||
| 2001 | Réthy LA, Kálmánchey R, Klujber V, Koós R, Fekete G. Acid sphingomyelinase deficiency in Beckwith Wiedemann syndrome. Pathology Oncology Research : Por. 6: 295-7. PMID 11173664 DOI: 10.1007/Bf03187335 | 0.376 | |||
| 1999 | Ferenczi A, Garami M, Kiss E, Pék M, Sasvári-Székely M, Barta C, Staub M, Sólyom J, Fekete G. Screening for mutations of 21-hydroxylase gene in Hungarian patients with congenital adrenal hyperplasia. The Journal of Clinical Endocrinology and Metabolism. 84: 2369-72. PMID 10404805 DOI: 10.1210/Jcem.84.7.5835 | 0.624 | |||
| 1997 | Garami M, Ferenczi A, Kiss E, Sasváry-Székely M, Sólyom J, Fekete G. Molecular Genotype in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency in Hungarian Population 74 Pediatric Research. 42: 397-397. DOI: 10.1203/00006450-199709000-00094 | 0.602 | |||
| 1996 | Urbán Z, Helms C, Peyrol S, Fekete G, Csiszar K, Bonnet D, Munnich A, Donis-Keller H, Boyd CD. Williams syndrome is characterized by 1 megabase deletions on 7q encompassing the elastin gene Matrix Biology. 15: 184. DOI: 10.1016/S0945-053X(96)90077-3 | 0.303 | |||
| 1994 | Sahota A, Chen J, Bye S, Jaing J, Berenyi M, Fekete G, Tischfield JA. Occurrence of a missense mutation in one allele and a seven basepair deletion in the other allele in a patient with adenine phosphoribosyltransferase deficiency. Human Mutation. 3: 315-7. PMID 7912608 DOI: 10.1002/Humu.1380030324 | 0.329 | |||
| 1993 | Hanson IM, Seawright A, Hardman K, Hodgson S, Zaletayev D, Fekete G, Heyningen Vv. PAX6 mutations in aniridia Human Molecular Genetics. 2: 915-920. PMID 8364574 DOI: 10.1093/Hmg/2.7.915 | 0.336 | |||
| 1990 | Wang T, Okano Y, Eisensmith RC, Fekete G, Schuler D, Berencsi G, Nasz I, Woo SLC. Molecular genetics of PKU in Eastern Europe: A nonsense mutation associated with haplotype 4 of the phenylalanine hydroxylase gene Somatic Cell and Molecular Genetics. 16: 85-90. PMID 2309142 DOI: 10.1007/Bf01650483 | 0.335 | |||
| 1988 | Czeizel A, Kovács M, Kiss P, Méhes K, Szabo L, Oláh E, Kosztolányi G, Szemere G, Kovács H, Fekete G. A nationwide evaluation of multiple congenital abnormalities in Hungary Genetic Epidemiology. 5: 183-202. PMID 3262553 DOI: 10.1002/Gepi.1370050305 | 0.338 | |||
| 1986 | Boyd P, Heyningen Vv, Seawright A, Fekete G, Hastie N. Use of catalase polymorphisms in the study of sporadic aniridia Human Genetics. 73: 171-174. PMID 3013756 DOI: 10.1007/Bf00291609 | 0.306 | |||
| 1986 | Fekete G, Réthy LA, Kardos G, Batta I, Révész T, Schuler D. 67 Association Of Congenital Malformations And Minor Anomalies In Children With Malignancies Pediatric Research. 20: 1045-1045. DOI: 10.1203/00006450-198610000-00121 | 0.334 | |||
| 1983 | Kardos G, Révész T, Bulin A, Fekete G, Vargha M, Schuler D. Leukaemia in children with Down's syndrome. Oncology. 40: 280-283. PMID 6223254 DOI: 10.1159/000225743 | 0.303 | |||
| 1979 | Schuler D, Dobos M, Fekete G, Miltényi M, Kalmár L. Chromosome mutations and chromosome stability in children treated with different regimes of immunosuppressive drugs. Human Heredity. 29: 100-105. PMID 437790 DOI: 10.1159/000153024 | 0.327 | |||
| 1976 | Dobos M, Fekete G, Schuler D, Kerpel-Fronius E. Chromosome Instability During Immunsuppressive Treatment Pediatric Research. 10: 556-556. DOI: 10.1203/00006450-197605000-00013 | 0.337 | |||
| 1974 | Fekete G, Dobos M, Schuler D, Kerpel-Fronius E. Mutability in Down's syndrome Pediatric Research. 8: 915-915. DOI: 10.1203/00006450-197411000-00097 | 0.349 | |||
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