Hall BD - Search Results

1

Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalities.

Moore CA, Toriello HV, Abuelo DN, Bull MJ, Curry CJ, Hall BD, Higgins JV, Stevens CA, Twersky S, Weksberg R, Dobyns WB. Moore CA, et al. Among authors: hall bd. Am J Med Genet. 1997 May 2;70(1):67-73. Am J Med Genet. 1997. PMID: 9129744

2

The Potter sequence: a clinical analysis of 80 cases.

Curry CJ, Jensen K, Holland J, Miller L, Hall BD. Curry CJ, et al. Among authors: hall bd. Am J Med Genet. 1984 Dec;19(4):679-702. doi: 10.1002/ajmg.1320190408. Am J Med Genet. 1984. PMID: 6393764

3

Partial trisomy for the distal long arm of chromosome 5 (region q34 leads to qter). A new clinically recognizable syndrome.

Curry CJ, Loughman WD, Francke U, Hall BD, Golbus MS, Derstine J, Epstein CJ. Curry CJ, et al. Among authors: hall bd. Clin Genet. 1979 May;15(5):454-61. Clin Genet. 1979. PMID: 445868

4

Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome.

Curry CJ, Hall BD. Curry CJ, et al. Among authors: hall bd. Birth Defects Orig Artic Ser. 1979;15(5B):253-63. Birth Defects Orig Artic Ser. 1979. PMID: 526581 No abstract available.

5

Patterns of multiple malformations in infants of diabetic mothers.

Grix A Jr, Curry C, Hall BD. Grix A Jr, et al. Among authors: hall bd. Birth Defects Orig Artic Ser. 1982;18(3 Pt A):55-77. Birth Defects Orig Artic Ser. 1982. PMID: 7126799 No abstract available.

6

Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.

Feingold M, Hall BD, Lacassie Y, Martínez-Frías ML. Feingold M, et al. Among authors: hall bd. Am J Med Genet. 1997 Mar 31;69(3):245-9. Am J Med Genet. 1997. PMID: 9096752

7

Meier-Gorlin syndrome: report of eight additional cases and review.

Bongers EM, Opitz JM, Fryer A, Sarda P, Hennekam RC, Hall BD, Superneau DW, Harbison M, Poss A, van Bokhoven H, Hamel BC, Knoers NV. Bongers EM, et al. Among authors: hall bd. Am J Med Genet. 2001 Aug 1;102(2):115-24. doi: 10.1002/ajmg.1452. Am J Med Genet. 2001. PMID: 11477602 Review.

8

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

9

Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and review.

Pivnick EK, Angle B, Kaufman RA, Hall BD, Pitukcheewanont P, Hersh JH, Fowlkes JL, Sanders LP, O'Brien JM, Carroll GS, Gunther WM, Morrow HG, Burghen GA, Ward JC. Pivnick EK, et al. Among authors: hall bd. Am J Med Genet. 2000 Jan 17;90(2):131-40. Am J Med Genet. 2000. PMID: 10607952 Review.

10

Pleiotropy in Coffin-Lowry syndrome: sensorineural hearing deficit and premature tooth loss as early manifestations.

Hartsfield JK Jr, Hall BD, Grix AW, Kousseff BG, Salazar JF, Haufe SM. Hartsfield JK Jr, et al. Among authors: hall bd. Am J Med Genet. 1993 Mar 1;45(5):552-7. doi: 10.1002/ajmg.1320450505. Am J Med Genet. 1993. PMID: 7681250

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