Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Maxim, Parizel"'
Autor:
Yves Jacquemyn, Cecile Colpaert, Bart Loeys, Heiko Reutter, Maxim Parizel, Bettina Blaumeiser, Katrien Janssens, Paul Ramaekers, Catharina von Lowtzow, Yves Leroy
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 100:797-800
Background Bladder exstrophy is a rare malformation. Prenatal diagnosis is usually an incidental finding on routine ultrasound examination. Triple-X syndrome (karyotype 47,XXX) is the most frequent sex chromosome aneuploidy in live-born females (appr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f146ea6b5275f2f253946729c76d9d3
https://doi.org/10.1002/bdra.23299
https://doi.org/10.1002/bdra.23299
Autor:
Paul, Ramaekers, Bart, Loeys, Catharina, von Lowtzow, Heiko, Reutter, Yves, Leroy, Cécile, Colpaert, Bettina, Blaumeiser, Katrien, Janssens, Maxim, Parizel, Yves, Jacquemyn
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 100(10)
Bladder exstrophy is a rare malformation. Prenatal diagnosis is usually an incidental finding on routine ultrasound examination. Triple-X syndrome (karyotype 47,XXX) is the most frequent sex chromosome aneuploidy in live-born females (approximately 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f16d52b13109787dae312c5d099ed8c8
https://pubmed.ncbi.nlm.nih.gov/25200913
https://pubmed.ncbi.nlm.nih.gov/25200913