Trisomy of chromosome 20
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1976.tb01595.x/fullpdf
Reference36 articles.
1. Long arm deletion of 19/20 chromosomes;Ahmed;Lancet,1972
2. Familial translocation involving chromosomes 6, 14, and 20, identified by quinacrine fluorescence;Allderdice;Hum. Genet.,1971
3. A ring-20 chromosome;Atkins;J. med. Genet.,1972
4. Association between congenital heart malformation and chromosomal variations;Book;Acta paediat. (Uppsala),1961
5. Les aberrations chromosomiques dam les avortements spontantés humains;Boué;Compt. Rend.,1966
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1. Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues;European Journal of Medical Genetics;2010-07
2. Pallister-Killian syndrome [i(12p)]: first pre-natal diagnosis using cordocentesis in the second trimester confirmed by in situ hybridization;Clinical Genetics;2008-06-28
3. Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus;Clinical Genetics;2008-06-28
4. Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicism;Clinical Genetics;2008-06-28
5. Case report: partial trisomy 20q (20q13.13→qter);Clinical Genetics;2008-04-23
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