Related Experiment Videos
Familial occurrence of chromosome variant 17ph+
Clinical Genetics
|July 1, 1977
Abstract:
A structural chromosome variant 17ph+ was found in a high genetic risk family. The authors consider the possibility of a causal connection between minor structural changes in the karyotype and congenital defects appearing in one member of the family.
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
The Floating-Harbor syndrome: two affected siblings in a family.
Clinical genetics·1996
XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning.
Genetic counseling (Geneva, Switzerland)·1995
Tetrasomy 9p: prenatal diagnosis and fetopathological findings in a second trimester male fetus.
Annales de genetique·1994
Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years).
Genetic counseling (Geneva, Switzerland)·1993
Duplication in the long arm of the X-chromosome associated with spastic paraparesis and premature menopause.
Genetic counseling (Geneva, Switzerland)·1993
The characteristic phenotype of distal 9q3 trisomy is due to duplication of band 9q32.
Genetic counseling (Geneva, Switzerland)·1993
Chlamydia trachomatis incidence in relation to vaginal microbiota dynamics, immunogenetics and exposures in a cohort of young student women in France.
The Journal of infectious diseases·2026
Exosome-Related Pathogenic Genes in Adenomyosis: A Multi-Omics Mendelian Randomization Study.
Omics : a journal of integrative biology·2026
Cognitive performance and neuroimaging markers across the glycemic spectrum in multiethnic Asian older adults.
Journal of internal medicine·2026