Genetic counseling in families with inherited balanced translocations: experience with 36 families
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb02965.x/fullpdf
Reference21 articles.
1. Trisomy 10p due to t(5;10)(p15;p11) segregation in a large sibship;Back;Hum. Genet.,1978
2. Two cases of partial trisomy 10q in the same family caused by parental direct insertion ins(15;10)(q15;q24q26);Back;Ann. Genet.,1979
3. Familiäre 2/C-Translokation: 46, XY, t(2p-;Cp+) und 46, XX Cp +;Bender;Hum. Genet.,1969
4. Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of European collaborative prenatal diagnosis centres;Daniel;Prenatal Diagnosis,1986
5. Decline in the predicted incidence of Huntington's chorea associated with systematic genetic counseling and family support;Harper;Lancet,1981
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1. Psychosocial Responses to being Identified as a Balanced Chromosomal Translocation Carrier: a Qualitative Investigation of Parents in Japan;Journal of Genetic Counseling;2015-03-20
2. Attitudes of physicians and patients towards disclosure of genetic information to spouse and first-degree relatives: a case study from Turkey;BMC Medical Ethics;2014-05-16
3. Prenatally detected de novo apparently balanced chromosomal rearrangements: the effect on maternal worry, family functioning and intent of disclosure;Prenatal Diagnosis;2014-04-25
4. A family genetic risk communication framework: guiding tool development in genetics health services;Journal of Community Genetics;2013-01-15
5. Family Communication of Genomic Information;Handbook of Genomics and the Family;2010
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