Trisomy 18q: 46, XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46, XY,-13,+der(13)/t(13;18)(q32;q11)-Reference-Cited by-同舟云学术

Trisomy 18q: 46, XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46, XY,-13,+der(13)/t(13;18)(q32;q11)

Published:2008-04-23 Issue:4 Volume:18 Page:233-238
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Murthy D. S. Krishna,Patel Z. M.,Ambani L. M.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1980.tb00879.x/fullpdf

Reference21 articles.

1. 47, XX, + der(18)(p24;q21)mat: a distinct partial trisomy 18q syndrome;Bass;J. med. Genet.,1975

2. The E-trisomy (trisomy 17-18) resulting from a maternal chromosomal translocation;Brodie;Canad. med. Ass. J.,1962

3. Trisomie partielle 18q par translocation familiale t(18q-; 13q+);Castel;Lyon Med.,1975

4. Familial dicentric translocation t(13;18)(p13;p11.2) ascertained by recurrent miscarriages;Daniel;J med. Genet.,1979

5. The trisomy 18 syndrome with an E/G translocation;Dziekanowska;Hum. Genet.,1976

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein to 18q22.3;American Journal of Medical Genetics;1996-04-09

2. Partial trisomy 18 with minimal anomalies: Lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18;American Journal of Medical Genetics;1990-08

3. Deletion 9p, duplication 18q in two sisters resulting from a maternal (9;18) (p22;q21.3) translocation;American Journal of Medical Genetics;1988-12

4. Phenotype-karyotype correlations in dup(18q): Report of a case and review;American Journal of Medical Genetics;1985-07

5. Trisomy 21 q: 46,XX,21s+/47,XX,+21q−(q22→qter) mosaicism (de novo) in a down syndrome child;The Indian Journal of Pediatrics;1984-05