Prenatal diagnosis of familial ring 21 chromosome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference19 articles.
1. A male infant with holoprosencephaly, associated with ring chromosome 21
2. (1991). The ACT Cytogenetics Manual, 2nd edn, New York: Raven Press, 161–163.
3. Inheritance of a ring 14 chromosome.
4. Ring chromosome 21 in healthy persons: different consequencies in females and in males
5. Acute lymphoblastic leukemia in a child with constitutional ring chromosome 21
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2. Ring Chromosome 21;Human Ring Chromosomes;2024
3. B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 21;Cytogenetic and Genome Research;2022
4. Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion;Taiwanese Journal of Obstetrics and Gynecology;2021-01
5. Constitutional abnormalities of chromosome 21 predispose to iAMP21-acute lymphoblastic leukaemia;European Journal of Medical Genetics;2016-03
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