Gilbert EF - Search Results

1

Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal disease.

Elejalde BR, Holguin J, Valencia A, Gilbert EF, Molina J, Marin G, Arango LA. Elejalde BR, et al. Among authors: gilbert ef. Am J Med Genet. 1979;3(1):65-80. doi: 10.1002/ajmg.1320030112. Am J Med Genet. 1979. PMID: 474620

2

Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.

Elejalde BR, Opitz JM, de Elejalde MM, Gilbert EF, Abellera M, Meisner L, Lebel RR, Hartigan JM. Elejalde BR, et al. Among authors: gilbert ef. Am J Med Genet. 1984 Apr;17(4):723-30. doi: 10.1002/ajmg.1320170403. Am J Med Genet. 1984. PMID: 6539070

3

Manifestations of pseudoxanthoma elasticum during pregnancy: a case report and review of the literature.

Elejalde BR, de Elejalde MM, Samter T, Burgess J, Lombardi J, Gilbert EF. Elejalde BR, et al. Among authors: gilbert ef. Am J Med Genet. 1984 Aug;18(4):755-62. doi: 10.1002/ajmg.1320180422. Am J Med Genet. 1984. PMID: 6385710

4

Acrocephalopolydactylous dysplasia.

Elejalde BR, Giraldo C, Jimenez R, Gilbert EF. Elejalde BR, et al. Among authors: gilbert ef. Birth Defects Orig Artic Ser. 1977;13(3B):53-67. Birth Defects Orig Artic Ser. 1977. PMID: 890100 No abstract available.

5

Clinicopathologic conference: a three-month-old infant with failure to thrive, hepatomegaly, and neurological impairment.

Friedman A, Bethzhold J, Hong R, Gilbert EF, Viseskul C, Opitz JM. Friedman A, et al. Among authors: gilbert ef. Am J Med Genet. 1980;7(2):171-86. doi: 10.1002/ajmg.1320070210. Am J Med Genet. 1980. PMID: 7468646 No abstract available.

6

The Johanson-Blizzard syndrome: case report and autopsy findings.

Daentl DL, Frías JL, Gilbert EF, Opitz JM. Daentl DL, et al. Among authors: gilbert ef. Am J Med Genet. 1979;3(2):129-35. doi: 10.1002/ajmg.1320030203. Am J Med Genet. 1979. PMID: 474625

7

Simpson-Golabi-Behmel syndrome: follow-up of the Michigan family.

Opitz JM, Herrmann J, Gilbert EF, Matalon R. Opitz JM, et al. Among authors: gilbert ef. Am J Med Genet. 1988 May-Jun;30(1-2):301-8. doi: 10.1002/ajmg.1320300131. Am J Med Genet. 1988. PMID: 3177456

8

Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG family.

Opitz JM, Kaveggia EG, Adkins WN Jr, Gilbert EF, Viseskul C, Pettersen JC, Blumberg B. Opitz JM, et al. Among authors: gilbert ef. Am J Med Genet. 1982 Jun;12(2):147-54. doi: 10.1002/ajmg.1320120205. Am J Med Genet. 1982. PMID: 7201743

9

The dup(3q) syndrome: report of eight cases and review of the literature.

Steinbach P, Adkins WN Jr, Caspar H, Dumars KW, Gebauer J, Gilbert EF, Grimm T, Habedank M, Hansmann I, Herrmann J, Kaveggia EG, Langenbeck U, Meisner LF, Najafzadeh TM, Opitz JM, Palmer CG, Peters HH, Scholz W, Tavares AS, Wiedeking C. Steinbach P, et al. Among authors: gilbert ef. Am J Med Genet. 1981;10(2):159-77. doi: 10.1002/ajmg.1320100210. Am J Med Genet. 1981. PMID: 7315873

10

Familial agnathia-holoprosencephaly.

Pauli RM, Pettersen JC, Arya S, Gilbert EF. Pauli RM, et al. Among authors: gilbert ef. Am J Med Genet. 1983 Apr;14(4):677-98. doi: 10.1002/ajmg.1320140411. Am J Med Genet. 1983. PMID: 6846401

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

237 results

Search Page