Crossing-over during human spermatogenesis visualized cytologically
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00304562.pdf
Reference18 articles.
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2. Bardhan S, Singh DN, Davis K (1981) Polymorphism in chromosome 4. Clin Genet 20:44?47
3. Craig-Holmes AP, Moore FB, Shaw MW (1975) Polymorphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing-over. Am J Hum Genet 27:179?189
4. Engel E (1980) A new genetic concept: Uniparental disomy and its potential effect, isodisomy. Am J Med Genet 6:137?143
5. Kirkels VGH, Hustinx WJ, Scheres JMJC (1980) Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter. Clin Genet 18:456?461
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1. De novo c.2455C>T mutation of NPR2 gene in a fetus with shortened long bones and a ventricular septal defect conceived by a mother with a fragile site at 16q22.1 and a father with a rare heterochromatic variant of chromosome 4 from Vietnam;Molecular Genetics & Genomic Medicine;2021-03-13
2. Partial deletion of 4p in fetal cells not present in chorionic villi;Clinical Genetics;2008-04-23
3. A rare heterochromatic variant of chromosome 4.;Journal of Medical Genetics;1984-12-01
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