Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.

Zackai, E H

Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction. [electronic resource] - American journal of medical genetics 1980 - 507-21 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

0148-7299

10.1002/ajmg.1320070412 doi


Abnormalities, Multiple--genetics
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, 6-12 and X
Female
Humans
Infant
Infant, Newborn
Intellectual Disability--genetics
Karyotyping
Male
Meiosis
Pedigree
Phenotype
Translocation, Genetic
Trisomy