Shaw GM - Search Results

1

Copy number variants in hypoplastic right heart syndrome.

Giannakou A, Sicko RJ, Kay DM, Zhang W, Romitti PA, Caggana M, Shaw GM, Jelliffe-Pawlowski LL, Mills JL. Giannakou A, et al. Among authors: shaw gm. Am J Med Genet A. 2018 Dec;176(12):2760-2767. doi: 10.1002/ajmg.a.40527. Epub 2018 Oct 5. Am J Med Genet A. 2018. PMID: 30289599

2

Risk of mental retardation among children born with birth defects.

Jelliffe-Pawlowski LL, Shaw GM, Nelson V, Harris JA. Jelliffe-Pawlowski LL, et al. Among authors: shaw gm. Arch Pediatr Adolesc Med. 2003 Jun;157(6):545-50. doi: 10.1001/archpedi.157.6.545. Arch Pediatr Adolesc Med. 2003. PMID: 12796234

3

Risks for severe mental retardation occurring in isolation and with other developmental disabilities.

Jelliffe-Pawlowski LL, Shaw GM, Nelson V, Harris JA. Jelliffe-Pawlowski LL, et al. Among authors: shaw gm. Am J Med Genet A. 2005 Jul 15;136(2):152-7. doi: 10.1002/ajmg.a.30801. Am J Med Genet A. 2005. PMID: 15940698

4

Infant C677T MTHFR polymorphism and severe mental retardation.

Shaw GM, Jelliffe-Pawlowski L, Nelson V, Zhu H, Harris JA, Finnell RH. Shaw GM, et al. Birth Defects Res A Clin Mol Teratol. 2007 Jan;79(1):24-6. doi: 10.1002/bdra.20321. Birth Defects Res A Clin Mol Teratol. 2007. PMID: 17149733

5

Population-based analysis of left- and right-sided diaphragmatic hernias demonstrates different frequencies of selected additional anomalies.

Slavotinek AM, Warmerdam B, Lin AE, Shaw GM. Slavotinek AM, et al. Among authors: shaw gm. Am J Med Genet A. 2007 Dec 15;143A(24):3127-36. doi: 10.1002/ajmg.a.32100. Am J Med Genet A. 2007. PMID: 18008313

6

Agenesis of the corpus callosum in California 1983-2003: a population-based study.

Glass HC, Shaw GM, Ma C, Sherr EH. Glass HC, et al. Among authors: shaw gm. Am J Med Genet A. 2008 Oct 1;146A(19):2495-500. doi: 10.1002/ajmg.a.32418. Am J Med Genet A. 2008. PMID: 18642362 Free PMC article.

7

The population-based prevalence of achondroplasia and thanatophoric dysplasia in selected regions of the US.

Waller DK, Correa A, Vo TM, Wang Y, Hobbs C, Langlois PH, Pearson K, Romitti PA, Shaw GM, Hecht JT. Waller DK, et al. Among authors: shaw gm. Am J Med Genet A. 2008 Sep 15;146A(18):2385-9. doi: 10.1002/ajmg.a.32485. Am J Med Genet A. 2008. PMID: 18698630 Free PMC article.

8

A maternally inherited chromosome 18q22.1 deletion in a male with late-presenting diaphragmatic hernia and microphthalmia-evaluation of DSEL as a candidate gene for the diaphragmatic defect.

Zayed H, Chao R, Moshrefi A, Lopezjimenez N, Delaney A, Chen J, Shaw GM, Slavotinek AM. Zayed H, et al. Among authors: shaw gm. Am J Med Genet A. 2010 Apr;152A(4):916-23. doi: 10.1002/ajmg.a.33341. Am J Med Genet A. 2010. PMID: 20358601 Free PMC article.

9

Folic acid in early pregnancy: a public health success story.

Obican SG, Finnell RH, Mills JL, Shaw GM, Scialli AR. Obican SG, et al. Among authors: shaw gm. FASEB J. 2010 Nov;24(11):4167-74. doi: 10.1096/fj.10-165084. Epub 2010 Jul 14. FASEB J. 2010. PMID: 20631328 Free PMC article.

10

Discovery of genetic susceptibility factors for human birth defects: an opportunity for a National Agenda.

Olshan AF, Hobbs CA, Shaw GM. Olshan AF, et al. Among authors: shaw gm. Am J Med Genet A. 2011 Aug;155A(8):1794-7. doi: 10.1002/ajmg.a.34103. Epub 2011 Jul 7. Am J Med Genet A. 2011. PMID: 21739590

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