Trisomy 3 mosaicism in a patient with Bartter syndrome.
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference3 articles.
1. Trisomy 3 mosaiicism in i live-born infant;N, Straitiaki-Benetou M.Kalpini-Mavrou A.Maltsianiotis;Cliit Genet
2. Humani(c3. Inheritaince of Banrtter synidrome;Percira, R.; wcrsch J, Van;Alm J Med Geniet,1983
3. Inheritaince of Banrtter synidrome;Percira, R.; wcrsch J, Van;Alm J Med Geniet,1983
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1. A mosaic mutation in the CLCNKB gene causing Bartter syndrome: A case report;Frontiers in Pediatrics;2023-04-17
2. A case of constitutional trisomy 3 mosaicism in a teenage patient with mild phenotype;European Journal of Medical Genetics;2016-11
3. Trisomy 3 mosaicism in a 5-year-old boy with multiple anomalies: A very rare case;American Journal of Medical Genetics Part A;2016-03-23
4. Constitutional and Acquired Autosomal Aneuploidy;Clinics in Laboratory Medicine;2011-12
5. Prenatal diagnosis of trisomy 3 mosaicism in a fetus with severe IUGR;Prenatal Diagnosis;2010-06-24
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