Open AccessP–573 PGT-M for two or more disease carrier patients diagnosed after whole exome sequencing
Author(s) -
Burcu Kara,
Murat Çetinkaya,
Semra Kahraman
Publication year - 2021
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/deab130.572
Subject(s) - exome sequencing , genetic testing , exome , carrier testing , genetic counseling , genetics , consanguinity , disease , biology , preimplantation genetic diagnosis , prenatal diagnosis , medicine , mutation , gene , pregnancy , fetus
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