Detection of trisomy 21 in a fetus during the investigation for Tay Sachs disease; prenatal cytogenetic study should be performed associated with molecular or enzymatic studies
Bildiriler > Özet Bildiri · 2002
Yazarlar: Asude DURMAZ, G Sapmaz, Emin KARACA, T CANKAYA, E BORA, Muhsin Özgür ÇOĞULU, Cumhur GÜNDÜZ, WJ KLEIJER, Feriştah Ferda ÖZKINAY
European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Fransa, Uluslararası, Sözlü Sunum, Özet Bildiri, 2002-2002, Wos, cilt 10, ss 285-285