Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Rehana Kazi"'
Autor:
Donna Blumenthal, Rehana Kazi, Jessy Jacob, Arthur Fougner, Joyce E. Fox, Jessica G. Davis, Sandra Sturim, Ann-Leslie Zaslav, Guy Pierno, Meira Shaham
Publikováno v:
Prenatal Diagnosis. 24:693-696
Objectives To present the clinical, cytogenetic, and molecular cytogenetic findings of prenatally diagnosed trisomy 3 mosaicism. Case and Methods Trisomy 3 mosaicism is rare, and only two cases of prenatally diagnosed trisomy 3 mosaicism have been re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::623adf4ccf179c6f86b3ab86f6fae9bc
https://doi.org/10.1002/pd.963
https://doi.org/10.1002/pd.963
Autor:
Guy Pierno, Joyce E. Fox, Ann-Leslie Zaslav, Fakhry Alexander, Donna Blumenthal, Arthur Fougner, Geraldine Shikora, Jessy Jacob, Rehana Kazi
Publikováno v:
American Journal of Medical Genetics. :420-422
Heterochromatic chromosome polymorphisms have been extensively reported. Most are associated with C-band positive regions located on chromosomes 1, 9, 16, and Y. We report a prenatal case of a rare heterochromatic variant on chromosome 4. Amniocentes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4cd5112bd7c8590f45c15cf201f22de
https://doi.org/10.1002/ajmg.a.20594
https://doi.org/10.1002/ajmg.a.20594
Autor:
T. Shklooskaya, Joyce E. Fox, Ann-Leslie Zaslav, Jessy Jacob, R.S. Verma, S. Allan, D. Sohal, S.M. Kleyman, Rehana Kazi
Publikováno v:
American Journal of Medical Genetics. 107:174-176
Structural chromosome mosaicism is rare. We report a case of prenatal mosaicism for a deletion of chromosome 10(q23). To our knowledge, there are only three reports of prenatally diagnosed cases of del(10)(q23). Two of these cases were due to an inhe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d976e002d827b43e621cda6fde2f8dc0
https://doi.org/10.1002/ajmg.10112
https://doi.org/10.1002/ajmg.10112