Hall BD - Search Results

1

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: hall bd. J Pediatr. 1998 Sep;133(3):441-8. doi: 10.1016/s0022-3476(98)70284-7. J Pediatr. 1998. PMID: 9738731 Review.

2

Confirmation of the Cohen syndrome.

Carey JC, Hall BD. Carey JC, et al. Among authors: hall bd. J Pediatr. 1978 Aug;93(2):239-44. doi: 10.1016/s0022-3476(78)80504-6. J Pediatr. 1978. PMID: 671157

3

The Coffin-Siris syndrome: five new cases including two siblings.

Carey JC, Hall BD. Carey JC, et al. Among authors: hall bd. Am J Dis Child. 1978 Jul;132(7):667-71. doi: 10.1001/archpedi.1978.02120320027005. Am J Dis Child. 1978. PMID: 665592

4

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: hall bd. Nat Genet. 1996 Aug;13(4):492-4. doi: 10.1038/ng0896-492. Nat Genet. 1996. PMID: 8696350

5

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

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

6

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

James AW, Culver K, Hall B, Golabi M. James AW, et al. 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.

7

Expanded phenotype and ethnicity in Setleis syndrome.

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

8

Penetrance and variability in neurofibromatosis: a genetic study of 60 families.

Carey JC, Laub JM, Hall BD. Carey JC, et al. Among authors: hall bd. Birth Defects Orig Artic Ser. 1979;15(5B):271-81. Birth Defects Orig Artic Ser. 1979. PMID: 118780 No abstract available.

9

Parietal foramina clavicular hypoplasia. An autosomal dominant syndrome.

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

10

Beare-Stevenson cutis gyrata syndrome.

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

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