Golabi M - Search Results

1

Parietal foramina clavicular hypoplasia. An autosomal dominant syndrome.

Golabi M, Carey J, Hall BD. Golabi M, et al. Am J Dis Child. 1984 Jun;138(6):596-9. doi: 10.1001/archpedi.1984.02140440080022. Am J Dis Child. 1984. PMID: 6720648

2

Beare-Stevenson cutis gyrata syndrome.

Hall BD, Cadle RG, Golabi M, Morris CA, Cohen MM Jr. Hall BD, et al. Among authors: golabi m. Am J Med Genet. 1992 Sep 1;44(1):82-9. doi: 10.1002/ajmg.1320440120. Am J Med Genet. 1992. PMID: 1519658

3

A new X-linked multiple congenital anomalies/mental retardation syndrome.

Golabi M, Ito M, Hall BD. Golabi M, et al. Am J Med Genet. 1984 Jan;17(1):367-74. doi: 10.1002/ajmg.1320170130. Am J Med Genet. 1984. PMID: 6711604

4

A new case of a LUMBAR syndrome.

Golabi M, An AC, Lopez C, Lee L, Kwong M, Hall BD. Golabi M, et al. Am J Med Genet A. 2014 Jan;164A(1):204-7. doi: 10.1002/ajmg.a.36215. Epub 2013 Nov 20. Am J Med Genet A. 2014. PMID: 24259379 Review.

5

Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome.

Przylepa KA, Paznekas W, Zhang M, Golabi M, Bias W, Bamshad MJ, Carey JC, Hall BD, Stevenson R, Orlow S, Cohen MM Jr, Jabs EW. Przylepa KA, et al. Among authors: golabi m. Nat Genet. 1996 Aug;13(4):492-4. doi: 10.1038/ng0896-492. Nat Genet. 1996. PMID: 8696350

6

DOOR syndrome: clinical report, literature review and discussion of natural history.

James AW, Miranda SG, Culver K, Hall BD, Golabi M. James AW, et al. Among authors: golabi m. Am J Med Genet A. 2007 Dec 1;143A(23):2821-31. doi: 10.1002/ajmg.a.32054. Am J Med Genet A. 2007. PMID: 17994565

7

Expanded phenotype and ethnicity in Setleis syndrome.

Clark RD, Golabi M, Lacassie Y, Hall B, Seto S. Clark RD, et al. Among authors: golabi m. Am J Med Genet. 1989 Nov;34(3):354-7. doi: 10.1002/ajmg.1320340311. Am J Med Genet. 1989. PMID: 2596524

8

Costello syndrome: phenotype, natural history, differential diagnosis, and possible cause.

Johnson JP, Golabi M, Norton ME, Rosenblatt RM, Feldman GM, Yang SP, Hall BD, Fries MH, Carey JC. Johnson JP, et al. Among authors: golabi m. J Pediatr. 1998 Sep;133(3):441-8. doi: 10.1016/s0022-3476(98)70284-7. J Pediatr. 1998. PMID: 9738731 Review.

9

Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.

Curry CJ, Carey JC, Holland JS, Chopra D, Fineman R, Golabi M, Sherman S, Pagon RA, Allanson J, Shulman S, et al. Curry CJ, et al. Among authors: golabi m. Am J Med Genet. 1987 Jan;26(1):45-57. doi: 10.1002/ajmg.1320260110. Am J Med Genet. 1987. PMID: 3812577

10

Bifid tongue: a rare feature associated with infants of diabetic mother syndrome.

James AW, Culver K, Hall B, Golabi M. James AW, et al. Among authors: golabi m. Am J Med Genet A. 2007 Sep 1;143A(17):2035-9. doi: 10.1002/ajmg.a.31877. Am J Med Genet A. 2007. PMID: 17663469 Review.

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