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Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD)
Author(s) -
Zielenski J,
Patrizio P,
Markiewicz D,
Asch RH,
Tsui LC
Publication year - 1997
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1997)9:2<183::aid-humu13>3.0.co;2-z
Subject(s) - obstetrics and gynaecology , sick child , medical genetics , medicine , university hospital , gynecology , family medicine , pediatrics , genetics , biology , gene , pregnancy