Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος:	Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center
Συγγραφείς:	Sarac Sivrikoz, Tugba^{Aff1, IDs00404021061254_cor1}, Basaran, Seher^{Aff2, Aff3}, Has, Recep, Karaman, Birsen^{Aff2, Aff4}, Kalelioglu, Ibrahim Halil, Kirgiz, Melike, Altunoglu, Umut, Yuksel, Atil
Πηγή:	Archives of Gynecology and Obstetrics. 305(2):323-342
Βάση Δεδομένων:	Springer Nature Journals

Περιγραφή
ISSN:	09320067 14320711
DOI:	10.1007/s00404-021-06125-4