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Human Genetics|February 1, 1980
Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier motherA SchinzelWiener Klinische Wochenschrift|April 16, 1982
[The use of chromosome variants in clinical cytogenetics (author's transl)]A SchinzelHuman Genetics|January 1, 1981
Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22A SchinzelHelvetica Paediatrica Acta|July 1, 1980
A case of multiple skeletal anomalies, ectodermal dysplasia, and severe growth and mental retardationA SchinzelHuman Genetics|June 19, 1979
Possible trisomy 1q25 leads to 1q32 in a malformed girl with a de novo insertion in 1qA SchinzelProgress in Clinical and Biological Research|January 1, 1993
Karyotype-phenotype correlations in autosomal chromosomal aberrationsA SchinzelHuman Genetics|June 10, 1977
Partial trisomy 8q in half-sisters with distinct dysmorphic patterns not similar to the trisomy 8 mosaicism syndromeA SchinzelCytogenetics and Cell Genetics|February 15, 2001
Discrepancies in cytogenetic results between different tissues in two fetuses with Wolf- Hirschhorn syndromeA SchinzelPageof 25