A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1974.tb02256.x/fullpdf
Reference4 articles.
1. Precise identification of various chromosomal abnormalities;Hirschhorn;Ann. hum. Genet.,1973
2. Possible partial trisomy of a chromosome of group 6-X-12 and familial translocation heterozygosity in a child with congenital abnormalities;Jensen;Develop. Med. Child Neurol.,1967
3. Antenatal detection of partial C (6-12) trisomy;Kersey;Lancet,1971
4. Malformation associated with precocious synthesis of adult haemoglobin;Weller;Lancet,1966
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1. Distal trisomy 10q syndrome, report of a patient with duplicated q24.31 – qter, autism spectrum disorder and unusual features;Clinical Case Reports;2014-07-25
2. Chromosomal abnormalities associated with congenital contractures (arthrogryposis);Clinical Genetics;2008-06-28
3. Balanced reciprocal translocations: risk factors for aneuploid segregant viability;Clinical Genetics;2008-04-23
4. Ocular Findings in Partial Trisomy 10q Syndrome;American Journal of Ophthalmology;1988-07
5. Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).;Journal of Medical Genetics;1986-10-01
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