Klinefelter‘ syndrome and trisomy 18 in a newborn boy
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1978.tb01179.x/fullpdf
Reference18 articles.
1. Une observation de double aneuploidie chromosomique: trisomie 18 et XXY;Bach;Ann. Génét.,1973
2. The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability;Caspersson;Hereditas (Lund),1971
3. Double aneuploidy. Trisomy-18 and Klinefelter's syndrome;Cohen;Amer. J. Dis. Child.,1967
4. A new trisomie syndrome;Edwards;Lancet,1960
5. The prepubertal testicular lesion in chromatin-positive Klinefelter's syndrome (primary micro-orchidism) as seen in mentally handicapped;Ferguson-Smith;Lancet,1959
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1. Double aneuploidy with Edwards–Klinefelter syndromes (48,XXY,+18) of maternal origin: Prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb;Taiwanese Journal of Obstetrics and Gynecology;2011-12
2. Double aneuploidy of trisomy 18 and Klinefelter syndrome: prenatal diagnosis and perinatal outcome;Journal of Perinatal Medicine;2010-01-01
3. Chromosome examination of children, in two Danish counties, born during the period 1967-1978;Hereditas;2009-02-12
4. A child with double trisomy: 48,XYY, + 18;Hereditas;2009-02-12
5. Chromosome abnormalities in children, in two Danish counties, born during the period 1967-1978 Clinical data;Hereditas;2008-06-28
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