Ardinger HH - Search Results

1

Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate.

Ardinger HH, Buetow KH, Bell GI, Bardach J, VanDemark DR, Murray JC. Ardinger HH, et al. Am J Hum Genet. 1989 Sep;45(3):348-53. Am J Hum Genet. 1989. PMID: 2570526 Free PMC article.

2

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.

3

RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19.

Ardinger HH, Ardinger RH, Bell GI, Murray JC. Ardinger HH, et al. Among authors: ardinger rh. Nucleic Acids Res. 1988 Aug 25;16(16):8202. doi: 10.1093/nar/16.16.8202. Nucleic Acids Res. 1988. PMID: 2901721 Free PMC article. No abstract available.

4

Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO).

Shiang R, Lidral AC, Ardinger HH, Buetow KH, Romitti PA, Munger RG, Murray JC. Shiang R, et al. Among authors: ardinger hh. Am J Hum Genet. 1993 Oct;53(4):836-43. Am J Hum Genet. 1993. PMID: 8105683 Free PMC article.

5

Multidisciplinary treatment results for patients with isolated cleft palate.

Morris HL, Bardach J, Ardinger H, Jones D, Kelly KM, Olin WH, Wheeler J. Morris HL, et al. Plast Reconstr Surg. 1993 Oct;92(5):842-51. Plast Reconstr Surg. 1993. PMID: 8415965

6

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

7

HincII and KpnI RFLPs for laminin B1 (LAMB1) gene on chromosome 7.

Ardinger HH, Rose KM, Murray JC, Yamada Y. Ardinger HH, et al. Nucleic Acids Res. 1988 Sep 12;16(17):8742. doi: 10.1093/nar/16.17.8742. Nucleic Acids Res. 1988. PMID: 2901729 Free PMC article. No abstract available.

8

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC. Kondo S, et al. Among authors: ardinger hh. Nat Genet. 2002 Oct;32(2):285-9. doi: 10.1038/ng985. Epub 2002 Sep 3. Nat Genet. 2002. PMID: 12219090 Free PMC article.

9

Verification of the fetal valproate syndrome phenotype.

Ardinger HH, Atkin JF, Blackston RD, Elsas LJ, Clarren SK, Livingstone S, Flannery DB, Pellock JM, Harrod MJ, Lammer EJ, et al. Ardinger HH, et al. Am J Med Genet. 1988 Jan;29(1):171-85. doi: 10.1002/ajmg.1320290123. Am J Med Genet. 1988. PMID: 3125743 Review.

10

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.

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