Daack-Hirsch S - Search Results

1

Impaired FGF signaling contributes to cleft lip and palate.

Riley BM, Mansilla MA, Ma J, Daack-Hirsch S, Maher BS, Raffensperger LM, Russo ET, Vieira AR, Dodé C, Mohammadi M, Marazita ML, Murray JC. Riley BM, et al. Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4512-7. doi: 10.1073/pnas.0607956104. Epub 2007 Mar 6. Proc Natl Acad Sci U S A. 2007. PMID: 17360555 Free PMC article.

2

Maternal alcohol use and risk of orofacial cleft birth defects.

Munger RG, Romitti PA, Daack-Hirsch S, Burns TL, Murray JC, Hanson J. Munger RG, et al. Teratology. 1996 Jul;54(1):27-33. doi: 10.1002/(SICI)1096-9926(199607)54:1<27::AID-TERA4>3.0.CO;2-0. Teratology. 1996. PMID: 8916367

3

Clinical and epidemiologic studies of cleft lip and palate in the Philippines.

Murray JC, Daack-Hirsch S, Buetow KH, Munger R, Espina L, Paglinawan N, Villanueva E, Rary J, Magee K, Magee W. Murray JC, et al. Cleft Palate Craniofac J. 1997 Jan;34(1):7-10. doi: 10.1597/1545-1569_1997_034_0007_caesoc_2.3.co_2. Cleft Palate Craniofac J. 1997. PMID: 9003905

4

The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations.

Romitti PA, Munger RG, Murray JC, Daack-Hirsch S, Hanson JW, Burns TL. Romitti PA, et al. Eur J Epidemiol. 1998 Feb;14(2):129-38. doi: 10.1023/a:1007406313703. Eur J Epidemiol. 1998. PMID: 9556171

5

A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD.

Semina EV, Ferrell RE, Mintz-Hittner HA, Bitoun P, Alward WL, Reiter RS, Funkhauser C, Daack-Hirsch S, Murray JC. Semina EV, et al. Nat Genet. 1998 Jun;19(2):167-70. doi: 10.1038/527. Nat Genet. 1998. PMID: 9620774

6

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC. Lidral AC, et al. Am J Hum Genet. 1998 Aug;63(2):557-68. doi: 10.1086/301956. Am J Hum Genet. 1998. PMID: 9683588 Free PMC article.

7

Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate.

Yoshiura K, Machida J, Daack-Hirsch S, Patil SR, Ashworth LK, Hecht JT, Murray JC. Yoshiura K, et al. Genomics. 1998 Dec 1;54(2):231-40. doi: 10.1006/geno.1998.5577. Genomics. 1998. PMID: 9828125

8

Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts.

Romitti PA, Lidral AC, Munger RG, Daack-Hirsch S, Burns TL, Murray JC. Romitti PA, et al. Teratology. 1999 Jan;59(1):39-50. doi: 10.1002/(SICI)1096-9926(199901)59:1<39::AID-TERA9>3.0.CO;2-7. Teratology. 1999. PMID: 9988882

9

Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.

Schutte BC, Basart AM, Watanabe Y, Laffin JJ, Coppage K, Bjork BC, Daack-Hirsch S, Patil S, Dixon MJ, Murray JC. Schutte BC, et al. Am J Med Genet. 1999 May 21;84(2):145-50. doi: 10.1002/(sici)1096-8628(19990521)84:2<145::aid-ajmg11>3.0.co;2-l. Am J Med Genet. 1999. PMID: 10323740

10

Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts.

Barrow LL, van Bokhoven H, Daack-Hirsch S, Andersen T, van Beersum SE, Gorlin R, Murray JC. Barrow LL, et al. J Med Genet. 2002 Aug;39(8):559-66. doi: 10.1136/jmg.39.8.559. J Med Genet. 2002. PMID: 12161593 Free PMC article.

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