Gelb BD - Search Results

1

The genetics of congenital heart disease: a review of recent developments.

Weismann CG, Gelb BD. Weismann CG, et al. Among authors: gelb bd. Curr Opin Cardiol. 2007 May;22(3):200-6. doi: 10.1097/HCO.0b013e3280f629c7. Curr Opin Cardiol. 2007. PMID: 17413276 Review.

2

Molecular genetics of congenital heart disease.

Gelb BD. Gelb BD. Curr Opin Cardiol. 1997 May;12(3):321-8. doi: 10.1097/00001573-199705000-00014. Curr Opin Cardiol. 1997. PMID: 9243090 Review.

3

Clinical implications and possible association of malposition of the branch pulmonary arteries with DiGeorge syndrome and microdeletion of chromosomal region 22q11.

Recto MR, Parness IA, Gelb BD, Lopez L, Lai WW. Recto MR, et al. Among authors: gelb bd. Am J Cardiol. 1997 Dec 15;80(12):1624-7. doi: 10.1016/s0002-9149(97)00782-0. Am J Cardiol. 1997. PMID: 9416954

4

Recent advances in the understanding of genetic causes of congenital heart defects.

Gelb BD. Gelb BD. Front Biosci. 2000 Mar 1;5:D321-33. doi: 10.2741/gelb. Front Biosci. 2000. PMID: 10704426 Review.

5

Genetic basis of syndromes associated with congenital heart disease.

Gelb BD. Gelb BD. Curr Opin Cardiol. 2001 May;16(3):188-94. doi: 10.1097/00001573-200105000-00006. Curr Opin Cardiol. 2001. PMID: 11357015 Review.

6

Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation.

Zhao F, Weismann CG, Satoda M, Pierpont ME, Sweeney E, Thompson EM, Gelb BD. Zhao F, et al. Among authors: gelb bd. Am J Hum Genet. 2001 Oct;69(4):695-703. doi: 10.1086/323410. Epub 2001 Aug 14. Am J Hum Genet. 2001. PMID: 11505339 Free PMC article.

7

Exclusion of PTPN11 mutations in Costello syndrome: further evidence for distinct genetic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes.

Tartaglia M, Cotter PD, Zampino G, Gelb BD, Rauen KA. Tartaglia M, et al. Among authors: gelb bd. Clin Genet. 2003 May;63(5):423-6. doi: 10.1034/j.1399-0004.2003.00076.x. Clin Genet. 2003. PMID: 12752577

8

Genetic basis of congenital heart disease.

Gelb BD. Gelb BD. Curr Opin Cardiol. 2004 Mar;19(2):110-5. doi: 10.1097/00001573-200403000-00007. Curr Opin Cardiol. 2004. PMID: 15075735 Review.

9

PTPN11 mutations play a minor role in isolated congenital heart disease.

Weismann CG, Hager A, Kaemmerer H, Maslen CL, Morris CD, Schranz D, Kreuder J, Gelb BD. Weismann CG, et al. Among authors: gelb bd. Am J Med Genet A. 2005 Jul 15;136(2):146-51. doi: 10.1002/ajmg.a.30789. Am J Med Genet A. 2005. PMID: 15940693

10

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.

Pandit B, Sarkozy A, Pennacchio LA, Carta C, Oishi K, Martinelli S, Pogna EA, Schackwitz W, Ustaszewska A, Landstrom A, Bos JM, Ommen SR, Esposito G, Lepri F, Faul C, Mundel P, López Siguero JP, Tenconi R, Selicorni A, Rossi C, Mazzanti L, Torrente I, Marino B, Digilio MC, Zampino G, Ackerman MJ, Dallapiccola B, Tartaglia M, Gelb BD. Pandit B, et al. Among authors: gelb bd. Nat Genet. 2007 Aug;39(8):1007-12. doi: 10.1038/ng2073. Epub 2007 Jul 1. Nat Genet. 2007. PMID: 17603483

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