A familial Y-22 translocation in man
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Reference8 articles.
1. A strongly fluorescing abnormal chromosome in a malformed child;Bühler;Humangenetik,1971
2. Presumptive Y/D translocation in mixed gonadal dysgenesis;Federman;J. Med. Genet.,1967
3. The fluorescent pattern of normal chromosomes in biopsies of malignant lymphomas, and its computer display;Fleischmann;Hereditas,1972
4. Presumptive Y-15 and Y-22 translocation in two families;Friedrich;Hereditas,1972
5. Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocation;Fründ;Humangenetik,1972
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1. An infertile azoospermic male with 45,X karyotype and a unique complex (Y;14); (Y;22) translocation: cytogenetic and molecular characterization;Journal of Assisted Reproduction and Genetics;2018-06-02
2. Y/autosomal translocations;Clinical Genetics;2008-04-23
3. The identification of Y chromosome translocations following Distamycin A treatment;Clinical Genetics;2008-04-23
4. Human Y Chromosome Function in Male Germ Cell Development;Advances in Developmental Biology (1992);1996
5. Phenotype/Karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases;American Journal of Medical Genetics;1994-11-01
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