Angle B - Search Results

1

Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.

Angle B, Hersh JH. Angle B, et al. Am J Med Genet. 1997 Aug 8;71(2):211-4. Am J Med Genet. 1997. PMID: 9217224

2

Developmental field defects: coming together of associations and sequences during blastogenesis.

Hersh JH, Angle B, Fox TL, Barth RF, Bendon RW, Gowans G. Hersh JH, et al. Among authors: angle b. Am J Med Genet. 2002 Jul 15;110(4):320-3. doi: 10.1002/ajmg.10429. Am J Med Genet. 2002. PMID: 12116204

3

Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.

Angle B, Yen F, Hersh JH, Gowans G, Barch M. Angle B, et al. Am J Med Genet. 2002 Aug 15;111(3):307-12. doi: 10.1002/ajmg.10599. Am J Med Genet. 2002. PMID: 12210328

4

Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome.

Angle B, Yen F, Hersh JH, Gowans G. Angle B, et al. Am J Med Genet A. 2003 Feb 1;116A(4):376-80. doi: 10.1002/ajmg.a.10025. Am J Med Genet A. 2003. PMID: 12522795

5

Anophthalmia, intracerebral cysts, and cleft lip/palate: expansion of the phenotype in oculocerebrocutaneous syndrome?

Angle B, Hersh JH. Angle B, et al. Am J Med Genet. 1997 Jan 10;68(1):39-42. doi: 10.1002/(sici)1096-8628(19970110)68:1<39::aid-ajmg7>3.0.co;2-t. Am J Med Genet. 1997. PMID: 8986273

6

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: angle b. Am J Med Genet. 2000 Jan 17;90(2):131-40. Am J Med Genet. 2000. PMID: 10607952 Review.

7

Case of partial duplication 2q3 with characteristic phenotype: rare occurrence of an unbalanced offspring resulting from a parental pericentric inversion.

Angle B, Hersh JH, Yen F, Christensen KM. Angle B, et al. Am J Med Genet. 2000 Mar 13;91(2):126-30. doi: 10.1002/(sici)1096-8628(20000313)91:2<126::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10748411

8

XY gonadal dysgenesis associated with a multiple pterygium syndrome phenotype.

Angle B, Hersh JH, Yen F, Verdi GD. Angle B, et al. Am J Med Genet. 1997 Jan 10;68(1):7-11. Am J Med Genet. 1997. PMID: 8986268

9

Molecularly proven hypochondroplasia with cloverleaf skull deformity: a novel association.

Angle B, Hersh JH, Christensen KM. Angle B, et al. Clin Genet. 1998 Nov;54(5):417-20. doi: 10.1111/j.1399-0004.1998.tb03756.x. Clin Genet. 1998. PMID: 9842995

10

Predictive value of fetal ultrasonography in the diagnosis of a lethal skeletal dysplasia.

Hersh JH, Angle B, Pietrantoni M, Cook VD, Spinnato JA, Clark AL, Kurtzman JT, Bendon RW, Gerassimides A. Hersh JH, et al. Among authors: angle b. South Med J. 1998 Dec;91(12):1137-42. doi: 10.1097/00007611-199812000-00008. South Med J. 1998. PMID: 9853726

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