Ardinger HH - Search Results

1

Identification and evaluation of mental retardation.

Daily DK, Ardinger HH, Holmes GE. Daily DK, et al. Among authors: ardinger hh. Am Fam Physician. 2000 Feb 15;61(4):1059-67, 1070. Am Fam Physician. 2000. PMID: 10706158 Free article. Review.

2

Family history and clefting as major criteria for CHARGE syndrome.

Hughes SS, Welsh HI, Safina NP, Bejaoui K, Ardinger HH. Hughes SS, et al. Among authors: ardinger hh. Am J Med Genet A. 2014 Jan;164A(1):48-53. doi: 10.1002/ajmg.a.36192. Epub 2013 Nov 8. Am J Med Genet A. 2014. PMID: 24214489

3

Linkage localization of Börjeson-Forssman-Lehmann syndrome.

Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA. Mathews KD, et al. Among authors: ardinger hh. Am J Med Genet. 1989 Dec;34(4):470-4. doi: 10.1002/ajmg.1320340403. Am J Med Genet. 1989. PMID: 2624254

4

Total absence of ribs in a newborn with cerebrocostomandibular syndrome.

Lale S, Ardinger H, Mardis N, Changho S, Lancaster T, Singh V. Lale S, et al. Pediatr Dev Pathol. 2011 Mar-Apr;14(2):134-7. doi: 10.2350/09-11-0745-CR.1. Epub 2010 Jul 26. Pediatr Dev Pathol. 2011. PMID: 20658933

5

Comprehensive ZEB2 gene analysis for Mowat-Wilson syndrome in a North American cohort: a suggested approach to molecular diagnostics.

Saunders CJ, Zhao W, Ardinger HH. Saunders CJ, et al. Among authors: ardinger hh. Am J Med Genet A. 2009 Nov;149A(11):2527-31. doi: 10.1002/ajmg.a.33067. Am J Med Genet A. 2009. PMID: 19842203

6

Expanding the phenotype of oculoectodermal syndrome: possible relationship to encephalocraniocutaneous lipomatosis.

Ardinger HH, Horii KA, Begleiter ML. Ardinger HH, et al. Am J Med Genet A. 2007 Dec 15;143A(24):2959-62. doi: 10.1002/ajmg.a.31969. Am J Med Genet A. 2007. PMID: 17963257

7

Cardiovascular malformations in Smith-Lemli-Opitz syndrome.

Lin AE, Ardinger HH, Ardinger RH Jr, Cunniff C, Kelley RI. Lin AE, et al. Among authors: ardinger hh, ardinger rh jr. Am J Med Genet. 1997 Jan 31;68(3):270-8. Am J Med Genet. 1997. PMID: 9024558 Review.

8

CDKN1C mutations and genital anomalies.

Welsh HI, Stockley TL, Parkinson N, Ardinger HH. Welsh HI, et al. Among authors: ardinger hh. Am J Med Genet A. 2012 Jan;158A(1):265. doi: 10.1002/ajmg.a.34388. Epub 2011 Dec 2. Am J Med Genet A. 2012. PMID: 22140035 No abstract available.

9

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.

Murray JC, Nishimura DY, Buetow KH, Ardinger HH, Spence MA, Sparkes RS, Falk RE, Falk PM, Gardner RJ, Harkness EM, et al. Murray JC, et al. Among authors: ardinger hh. Am J Hum Genet. 1990 Mar;46(3):486-91. Am J Hum Genet. 1990. PMID: 2309700 Free PMC article.

10

Microcephaly in familial holoprosencephaly.

Ardinger HH, Bartley JA. Ardinger HH, et al. J Craniofac Genet Dev Biol. 1988;8(1):53-61. J Craniofac Genet Dev Biol. 1988. PMID: 3209679

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