Pericentric inversion of chromosome 16 in a large kindred: Spectrum of morbidity and mortality in offspring
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference16 articles.
1. A long-range restriction map between the α-globin complex and a marker closely linked to the polycystic kidney disease 1 (PKD1) locus
2. A review of the molecular genetics of the human alpha-globin gene cluster
3. A unique pattern of central nervous system leukemia in acute myelomonocytic leukemia associated with inv(16)(p13q22)
4. Multiple congenital anomalies syndrome with myopathy in chromosome 16 abnormality
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1. Constitutional pericentric inversion of chromosome 16, inv(16)(p13.1q22), mimicking acute myeloid leukemia;eJHaem;2022-10-20
2. Constitutional chromosome rearrangements that mimic the 2017 world health organization “acute myeloid leukemia with recurrent genetic abnormalities”: A study of three cases and review of the literature;Cancer Genetics;2019-01
3. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter);Taiwanese Journal of Obstetrics and Gynecology;2016-04
4. Recurrent Distal 16q Duplication and Terminal 22q Deletion: Prenatal Diagnosis and Genetic Counseling;Taiwanese Journal of Obstetrics and Gynecology;2010-12
5. Inherited pericentric inversion of chromosome 16 in chronic phase of chronic myeloid leukaemia;Leukemia Research;2006-01
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