Cytogenetic and molecular studies of trisomy 13.

Author:

Hassold T,Jacobs P A,Leppert M,Sheldon M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. Non-disjunction in trisomy 21: study of chromosomal heteromorphisms in 110 families;Mikkelsen, M.; Poulsen, H.; Grinsted, J.; Lange, A.;Ann Hum Genet

2. Factors involved in chromosomal nondisjunction: a European Collaborative Study supported by the EEC;Ayme, S.; Baccichetti, C.; Bricarelli, F.D.;Seventh International Congress of Human Genetics, 1986; I: C; Hum Genet; Origin of extra chromosome in Patau syndrome,1984

3. Parental origin of autosomal trisomies;Hassold, T.; Chiu, D.; Yamane, J.;Ann Hum Genet,1984

4. Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences;Antonarakis, S.E.; Kittur, S.D.; Metaxotou, C.; Watkins, P.C.; Patel, A.S.,1985

5. Animal cytology and evolution;White, M.J.D.,1973

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