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Klinische Padiatrie|July 1, 1989
[Psychological management of children with cancer and their families]H Wittmeyer, U KaufmannClinical Genetics|October 1, 1980
Interstitial deletion of the long arm of chromosome 1, del(1)(q21 leads to q25) in a profoundly retarded 8-year-old girl with multiple anomaliesA Schinzel, W SchmidHuman Genetics|January 1, 1979
Partial trisomy 7q and probable partial monosomy of 5p in the son of a mother with a reciprocal translocation between 5p and 7qA Schinzel, O TönzClinical Dysmorphology|July 1, 1993
A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndromeA Bottani, A SchinzelAmerican Journal of Medical Genetics|January 1, 1980
Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndromeA Schinzel, W SchmidOphthalmic Paediatrics and Genetics|June 1, 1990
Anophthalmia in a retarded girl with partial trisomy 4p and 22 following a maternal translocation, rcp(4;22)(p15.2;q11.2)A Schinzel, V D'ApuzzoEuropean Journal of Human Genetics : EJHG|September 12, 2000
Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46, XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndromeD Kotzot, A SchinzelAmerican Journal of Medical Genetics|October 2, 2001
Chromosome imbalances associated with epilepsyA Schinzel, D NiedristAmerican Journal of Medical Genetics|January 1, 1978
A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibsA Schinzel, A GiedionPageof 33