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pro vyhledávání: '"Diane L. Broome"'
Autor:
Pawel Stankiewicz, Swaroop Aradhya, Elizabeth Cameron, Danielle Martinet, Rolph Pfundt, Eliane Roulet, Angelo Selicorni, Jacques S. Beckmann, Bregje W.M. van Bon, Mira Irons, Sébastien Jacquemont, Lorraine Potocki, Barry Wolf, Melissa Bellini, Ankita Patel, Nine V A M Knoers, Annalisa Vetro, Scott B. Selleck, Han G. Brunner, James R. Lupski, Jorune Balciuniene, Sau Wai Cheung, Orsetta Zuffardi, Margherita Silengo, Sandesh C.S. Nagamani, Roberto Ciccone, Petr E. Jira, Gary Fruhman, Bert B.A. de Vries, Diane L Broome, Nicole de Leeuw, Brendan Lee
Publikováno v:
European Journal of Human Genetics, 19, 400-8
European Journal of Human Genetics, 19, 4, pp. 400-8
European Journal of Human Genetics, 19, 4, pp. 400-8
Item does not contain fulltext The genomic architecture of the 10q22q23 region is characterised by two low-copy repeats (LCRs3 and 4), and deletions in this region appear to be rare. We report the clinical and molecular characterisation of eight nove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4606689b6239d089a08cd086ecbc10f
http://hdl.handle.net/2318/80606
http://hdl.handle.net/2318/80606
Publikováno v:
American Journal of Obstetrics and Gynecology. 126:247-252
Needle puncture of the fetus has rarely been reported with midtrimester amniocentesis. This paper contains the report of five cases of needle scars in infants born after second-trimester amniocentesis for prenatal diagnosis of fetal genetic disorders