Molecular cytogenetic analysis of a familial pericentric inversion of chromosome 12
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03869.x/fullpdf
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4. Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p;Dauwerse;Cytogenet Cell Genet,1990
5. A cluster of alpha-2-macroglobulin-related genes (A2M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and a A2M pseudogene;Devriendt;Gene,1989
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1. Prenatal diagnosis of two different unbalanced forms of an inherited (Y;12) translocation;American Journal of Medical Genetics Part A;2009-12
2. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: Clinical, cytogenetic and molecular observations;European Journal of Medical Genetics;2007-05
3. Cryptic duplication of 12q24.33→qter in a child with Angelman syndrome—simultaneous occurrence of two unrelated cytogenetic events;American Journal of Medical Genetics Part A;2007
4. Pure direct duplication (12)(q24.1 → q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomalies;American Journal of Medical Genetics Part A;2006-02-01
5. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter);Prenatal Diagnosis;2006
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