Peri- and paracentric inversions in chromosome 12: Prenatal diagnosis and family study
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference13 articles.
1. Identification of human chromosomes by DNA-binding fluorescent agents
2. Danish Cytogenetic Central Registry 1979.
3. Quantitative analysis of high-resolution trypsin-Giemsa bands on human prometaphase chromosomes
4. Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.
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1. Paracentric inversions in man;Clinical Genetics;2008-04-23
2. Two cousins with partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of the chromosome 12;American Journal of Medical Genetics;2004
3. A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies;American Journal of Medical Genetics;2004
4. Development of Acute Lymphoblastic Leukemia with Translocation (4;11) in a Young Girl with Familial Pericentric Inversion 12;Cancer Genetics and Cytogenetics;1999-04
5. Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases;American Journal of Medical Genetics;1995-01-16
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