Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.-Reference-Cited by-同舟云学术

Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.

Published:1979-06-01 Issue:3 Volume:16 Page:225-226
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Rinaldi A,Archidiacono N,Rocchi M,Filippi G

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference5 articles.

1. Successive non-disjunction at first and second meiotic division of spermatogenesis: evidence of chromosomes and Xg;De la Chapelle, A.; Hortling, H.; Sanger, R.; Race, R.R.;Cytogenetics,1964

2. Paternal origin of an XXYY anomaly;Pfeiffer, R.A.; Korver, G.; Sanger, R.; Race, R.R.;Lancet,1966

3. Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia;Rinaldi, A.; Filippi, G.; Siniscalco, M.;American Journal of Human Genetics,1976

4. Xg groups and sex chromosome abnormalities in people of northern European ancestry: an addendum;Sanger, R.; Tippett, P.; Gavin, J.; Teesdale, P.; Daniels, G.L.;Journal ofMedical Genetics,1977

5. Failure to detect linkage between Xg and other X-borne loci in Sardinians;Siniscalco, M.; Filippi, G.; Latte, B.; Piomelli, S.; Rattazzi, M.; Gavin, J.; Sanger, R.; Race, R.R.;Annals ofHuman Genetics,1966

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