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American Journal of Medical Genetics|March 27, 1995
"C" trigonocephaly syndrome: report of a child with agenesis of the corpus callosum and tetralogy of Fallot, and reviewJ Glickstein, J Karasik, D G Caride, et al.American Journal of Medical Genetics|March 27, 1995
FISH analysis in Prader-Willi and Angelman syndrome patientsD Bettio, N Rizzi, D Giardino, et al.American Journal of Medical Genetics|March 27, 1995
Craniofacial and dental characteristics of Silver-Russell syndromeJ Kotilainen, P Hölttä, T Mikkonen, et al.American Journal of Medical Genetics|October 16, 1996
Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2M Li, E H Zackai, N Niikawa, et al.American Journal of Medical Genetics|October 16, 1996
Pallister-Killian syndrome: a mild case diagnosed by fluorescence in situ hybridization. Review of the literature and expansion of the phenotypeM M Bielanska, M M Khalifa, A M DuncanAmerican Journal of Medical Genetics|October 16, 1996
Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephalyJ R Sawyer, J L Lukacs, S J Hassed, et al.American Journal of Medical Genetics|October 16, 1996
Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differencesJ Mitchell, A Schinzel, S Langlois, et al.American Journal of Medical Genetics|October 2, 1996
Distinctive Menkes disease variant with occipital horns: delineation of natural history and clinical phenotypeV K Proud, H G Mussell, S G Kaler, et al.American Journal of Medical Genetics|October 2, 1996
Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cenS Schuffenhauer, A Kobelt, C Daumer-Haas, et al.American Journal of Medical Genetics|October 2, 1996
Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysisE Blennow, T H Bui, A Wallin, et al.Pageof 854