A Variant Chromosome 17 in a Mother with Repeated Abortions and a 46,XY/47,XXY Klinefelter Son
Author:
Publisher
Uppsala Medical Society
Subject
General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/03009737809179124
Reference21 articles.
1. SYMTOMATOLOGY IN SCHOOLBOYS WITH POSITIVE SEX CHROMATIN (THE KLINEFELTER SYNDROME)
2. A HOMOZYGOUS CHROMOSOMAL VARIANT
3. The XXY (Klinefelter's) syndrome in childhood: Detection and treatment
4. Differential binding of alkylating fluorochromes in human chromosomes
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1. Chromosome Heteromorphism (Summaries);Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017
2. Germ cell loss is associated with fading Lin28a expression in a mouse model for Klinefelter's syndrome;REPRODUCTION;2014-03
3. Chromosome 17;Human Chromosome Variation: Heteromorphism and Polymorphism;2011
4. Paternal non-disjunction in a 46, XY/ 47, XXY individual with a fragile 17p12 in the mother;Clinical Genetics;2008-04-23
5. Letter to the Editors;Clinical Genetics;2008-04-23
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