Robert Gorlin
Affiliations: |
Google:
"Robert Gorlin"Mean distance: 35622
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Zarate YA, Pacheco MC, Bove KE, et al. (2009) Phenotypic and microscopic description of a new case of Ermine phenotype. American Journal of Medical Genetics. Part A. 149: 1253-6 |
| Ng D, Thakker N, Corcoran CM, et al. (2004) Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. Nature Genetics. 36: 411-6 |
| Faivre L, Gorlin RJ, Wirtz MK, et al. (2003) In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome. Journal of Medical Genetics. 40: 34-6 |
| GORLIN RJ, CHAUDHRY AP. (2002) Oral melanotic pigmentation in polyostotic fibrous dysplasia, Albright's syndrome. Oral Surgery, Oral Medicine, and Oral Pathology. 10: 857-62 |
| Barrow LL, van Bokhoven H, Daack-Hirsch S, et al. (2002) Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts. Journal of Medical Genetics. 39: 559-66 |
| Dowling PA, Fleming P, Gorlin RJ, et al. (2001) The KBG syndrome, characteristic dental findings: a case report. International Journal of Paediatric Dentistry / the British Paedodontic Society [and] the International Association of Dentistry For Children. 11: 131-4 |
| Crutchfield CE, Geiger J, Gorlin RJ, et al. (2000) What syndrome is this? Pediatric Dermatology. 17: 484-6 |
| Gorlin RJ. (2000) Whistling face syndrome with normal hands. American Journal of Medical Genetics. 90: 255 |
| YUNIS JJ, GORLIN RJ. (1998) Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome. Chromosoma. 14: 146-53 |
| GORLIN RJ, PSAUME J. (1998) Orodigitofacial dysostosis--a new syndrome. A study of 22 cases. The Journal of Pediatrics. 61: 520-30 |