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American Journal of Medical Genetics. Part A|October 18, 2008
Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese populationIngo Kennerknecht, Nga Yee Ho, Virginia C N WongAmerican Journal of Medical Genetics. Part A|October 18, 2008
Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36Shoji Saito, Rie Kawamura, Tomoki Kosho, et al.American Journal of Medical Genetics. Part A|July 12, 2005
A report of three patients with an interstitial deletion of chromosome 15q24Lisa J Cushman, Wilfredo Torres-Martinez, Athena M Cherry, et al.American Journal of Medical Genetics. Part A|July 12, 2005
Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3Arjan P M de Brouwer, Hendrikus P M Kunst, Alice Krebsova, et al.American Journal of Medical Genetics. Part A|July 12, 2005
Plantar lipomatosis, unusual facies, and developmental delay: confirmation of Pierpont syndromeGrétel G Oudesluijs, Roel Hordijk, Maartje Boon, et al.American Journal of Medical Genetics. Part A|July 12, 2005
Epidemiologic characteristics of anophthalmia and bilateral microphthalmia among 2.5 million births in California, 1989-1997Gary M Shaw, Suzan L Carmichael, Wei Yang, et al.American Journal of Medical Genetics. Part A|August 16, 2005
Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndromeManinder Kaur, Cheryl DeScipio, Jennifer McCallum, et al.American Journal of Medical Genetics. Part A|August 10, 2005
Growth deficiency, facial anomalies, and brachydactyly (Frías syndrome): a second familyMaría Luisa Martínez-Frías, Joaquín Fernández Toral, Fermina López-Grondona, et al.American Journal of Medical Genetics. Part A|August 10, 2005
Novel amino acid substitution in the Y-position of collagen type II causes spondyloepimetaphyseal dysplasia congenitaJ Sulko, M Czarny-Ratajczak, A Wozniak, et al.American Journal of Medical Genetics. Part A|August 10, 2005
High prevalence of the W24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing lossAraceli Alvarez, Ignacio del Castillo, Manuela Villamar, et al.Pageof 929