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Birth Defects Research. Part A, Clinical and Molecular Teratology|August 12, 2016
Birth defects and neonatal morbidity caused by teratogen exposure after the embryonic periodAngela E Scheuerle, Arthur S Aylsworth
North Carolina Medical Journal|December 10, 2013
Direct-to-consumer genomic testing offers little clinical utility but appears to cause minimal harmStacie D Adams, James P Evans, Arthur S Aylsworth
American Journal of Medical Genetics. Part A|February 3, 2004
Submicroscopic deletion 9(q34.3) and duplication 19(p13.3): identified by subtelomere specific FISH probesDenise I Quigley, Kathleen Kaiser-Rogers, Arthur S Aylsworth, et al.
Clinics in Plastic Surgery|March 11, 2014
Classification, epidemiology, and genetics of orofacial cleftsStephanie E Watkins, Robert E Meyer, Ronald P Strauss, et al.
Ophthalmic Genetics|January 24, 2017
Ocular manifestations in the X-linked intellectual disability syndromesNatario L Couser, Maheer M Masood, Arthur S Aylsworth, et al.
Journal of Pediatric Hematology/Oncology|September 16, 2014
Genetics of hemangiomas, vascular malformations, and primary lymphedemaJulie Blatt, Cynthia M Powell, Craig N Burkhart, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 8, 2011
Autoimmune polyendocrinopathy associated with ring chromosome 18Nina Jain, Pamela J Reitnauer, Kathleen W Rao, et al.
American Journal of Medical Genetics. Part A|October 30, 2016
Camptodactyly and the 22q11.2 deletion syndromeNatario L Couser, Chetna K Pande, Jonathan M Walsh, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
A 137-kb deletion within the Potocki-Shaffer syndrome interval on chromosome 11p11.2 associated with developmental delay and hypotoniaNathan D Montgomery, Christie M Turcott, James H Tepperberg, et al.
American Journal of Epidemiology|October 7, 2008
Maternal body mass index and lifestyle exposures and the risk of bilateral renal agenesis or hypoplasia: the National Birth Defects Prevention StudyJennifer E Slickers, Andrew F Olshan, Anna Maria Siega-Riz, et al.
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