Showing results (241-250 of 392) with videos related to
Sort By:
Pageof 40
American Journal of Medical Genetics|April 1, 1983
Familial agnathia-holoprosencephalyR M Pauli, J C Pettersen, S Arya, et al.Experientia|January 15, 1979
Acetylsalicylic acid-induced morphological changes in the ductus arteriosus of the chick embryoS Ishikawa, M O Cheung, E F Gilbert, et al.Medical and Pediatric Oncology|January 1, 1983
Leukemia presenting as central nervous disease without bone marrow involvementD J Ganick, P M Sondel, E F Gilbert, et al.Human Molecular Genetics|February 1, 1997
A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3S S Chong, S D Pack, A V Roschke, et al.Journal of Medical Genetics|January 3, 2001
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14P Ungaro, S L Christian, J A Fantes, et al.Neurology|October 27, 1997
Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: a new X-linked mental retardation syndromeW B Dobyns, R Guerrini, D K Czapansky-Beilman, et al.American Journal of Medical Genetics|March 1, 1987
Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studiesJ M Opitz, J W Spranger, H R Stöss, et al.American Journal of Medical Genetics|May 3, 1996
Kniest dysplasia: radiologic, histopathological, and scanning electronmicroscopic findingsE Gilbert-Barnes, L O Langer, J M Opitz, et al.American Journal of Medical Genetics|January 1, 1980
Cerebroarthrodigital syndrome: a newly recognized formal genesis syndrome in three patients with apparent arthromyodysplasia and sacral agenesis, brain malformation and digital hypoplasiaJ W Spranger, A Schinzel, T Myers, et al.American Journal of Medical Genetics|October 21, 1999
Trisomy 2p syndrome: a fetus with anencephaly and postaxial polydactylyG K Hahm, R F Barth, G M Schauer, et al.Pageof 40