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American Journal of Medical Genetics. Part A|September 13, 2011
West syndrome associated with mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14Jun Tohyama, Toshiyuki Yamamoto, Kana Hosoki, et al.American Journal of Medical Genetics. Part A|September 13, 2011
Having a brother or sister with Down syndrome: perspectives from siblingsBrian G Skotko, Susan P Levine, Richard GoldsteinAmerican Journal of Medical Genetics. Part A|September 13, 2011
Visual processing in Noonan syndrome: dorsal and ventral stream sensitivityPaolo Alfieri, Laura Cesarini, Paola De Rose, et al.American Journal of Medical Genetics. Part A|September 13, 2011
New case of Primrose syndrome with mild intellectual disabilityRenata Posmyk, Ryszard Leśniewicz, Monika Chorąży, et al.American Journal of Medical Genetics. Part A|September 15, 2011
Bone density phenotypes in mice aneuploid for the Down syndrome critical regionLisa E Olson, Subburaman MohanAmerican Journal of Medical Genetics. Part A|August 5, 2011
The microcephaly-capillary malformation syndromeGhayda M Mirzaa, Alex R Paciorkowski, Christopher D Smyser, et al.American Journal of Medical Genetics. Part A|August 5, 2011
A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic featuresAndrew B Cyr, Manjunath Nimmakayalu, Susannah Q Longmuir, et al.American Journal of Medical Genetics. Part A|August 5, 2011
Two novel heterozygous mutations of EVC2 cause a mild phenotype of Ellis-van Creveld syndrome in a Chinese familyWenjing Shen, Dong Han, Jin Zhang, et al.American Journal of Medical Genetics. Part A|August 5, 2011
Familial cardiac valvulopathy due to filamin A mutationJonathan A Bernstein, Daniel Bernstein, Ute Hehr, et al.American Journal of Medical Genetics. Part A|August 5, 2011
Potential teratogenic effects of allopurinol: a case reportMariya Kozenko, David Grynspan, Titi Oluyomi-Obi, et al.Pageof 928