Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Aurora Popa"'
Publikováno v:
Perinatologia. 4:187-189
Prader-Willi syndrome is a consequence of several genetic defects in the 15q11-q13 region, including methylation changes, and is associated in newborns with hypotonia, poor suck, a reduced growth velocity, and developmental delay. We present the case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12c3e460c8d6b448854759bec7c68d2e
https://doi.org/10.26416/peri.4.4.2017.1435
https://doi.org/10.26416/peri.4.4.2017.1435
Publikováno v:
Perinatologia. 2:84
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7453c31029b17e6bd0255e61389bc6c
https://doi.org/10.26416/peri.1.2.2017.835
https://doi.org/10.26416/peri.1.2.2017.835
Autor:
Elena Mădălina Barbu, Maria Comănescu, Aurora Popa, Nicolae Cernea, Alexandru Comănescu, Ovidiu Costinel Sîrbu, Mihaela Hîrnău
Publikováno v:
Ginecologia.ro. 4:18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a756d8961ac73df8141c7f6c9fd43187
https://doi.org/10.26416/gine.18.4.2017.1325
https://doi.org/10.26416/gine.18.4.2017.1325