X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
Author:
Affiliation:
1. Universidade Estadual Paulista Júlio de Mesquita Filho, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v29n1/28167.pdf
Reference8 articles.
1. Rapid and accurate determination of (CAG)n repeats in the androgen receptor gene using polymerase chain reaction and automated fragment analysis;Bharaj BS;Clin Biochem,1999
2. A family showing translocation of a D/D reciprocal translocation and a case of regular 21 trisomy Dow's syndrome;Hamerton JL;Cytogenetics,1968
3. Possible interchromosomal effect in embryos generated by gametes from translocation carriers;Gianaroli L;Human Reproduction,2002
4. Parental origin of the X chromosome in a patient with a robertsonian translocation na Turner's syndrome;Krajinovic M;J Med Genet,1994
5. A case of Turner's syndrome with familial balanced translocation t(1;2) (q32;q21) mat;Kondo I;J Med Genet,1979
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1. Robertsonian translocation (13;14) and its clinical manifestations: a literature review;REPROD BIOMED ONLINE;2022
2. Robertsonian translocation (13;14) and its clinical manifestations: a literature review;Reproductive BioMedicine Online;2022-09
3. Study on the Effect of Socio-Demographic Factors on Different Congenital Disorders;Down Syndrome and Other Chromosome Abnormalities [Working Title];2021-10-06
4. The value of a simple method to decrease diagnostic errors in Turner syndrome: a case report;Journal of Medical Case Reports;2021-02-18
5. Cytogenetic and genomic analysis of a patient with turner syndrome and t(2;12): a case report;Molecular Cytogenetics;2020-11-13
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