Dicentric chromosome 13 and centromere inactivation

Author:

Schwartz Stuart,Palmer Catherine G.,Weaver David D.,Priest Jean

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference41 articles.

1. Al-Nassar KE (1979) The distribution of genetic markers and Q-band heteromorphisms in the Kuwaiti population. Ph. D. Thesis, Indiana University

2. Bartsch-Sandhoff M, Schade H (1973) Zwei subterminale Heterochromatinregionen bei einer seltenen Form einer 21/21-Translokation. Hum Genet 18:329?336

3. Berg JM, Gardner HA, Gardner RJM, Goh EG, Markovic VD, Simpson NE, Worton RG (1980) Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother. J Med Genet 17: 144?148

4. Cantu JM, Hernandez A, Plascencia L, Vaca G, Moller M, Rivera H (1980) Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation. Ann Genet (Paris) 23:183?186

5. de Grouchy J, Turleau C (1977) Clinical atlas of human chromosomes. John Wiley, New York

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