Zobrazeno 1 - 3
of 3
pro vyhledávání: '"paternal UPD(14)"'
Autor:
Rishika P. Sakaria, Roya Mostafavi, Stephen Miller, Jewell C. Ward, Eniko K. Pivnick, Ajay J. Talati
Publikováno v:
American Journal of Perinatology Reports, Vol 11, Iss 02, Pp e65-e75 (2021)
Kagami-Ogata syndrome (KOS) (OMIM #608149) is a genetic imprinting disorder affecting chromosome 14 that results in a characteristic phenotype consisting of typical facial features, skeletal abnormalities including rib abnormalities described as “c
Externí odkaz:
https://doaj.org/article/e2d5e1d826b44149b416ee8e77e425b1
Autor:
Stephen T. Miller, Jewell C. Ward, Roya Mostafavi, Eniko K. Pivnick, Ajay J. Talati, Rishika P. Sakaria
Publikováno v:
AJP Reports
American Journal of Perinatology Reports, Vol 11, Iss 02, Pp e65-e75 (2021)
American Journal of Perinatology Reports, Vol 11, Iss 02, Pp e65-e75 (2021)
Kagami-Ogata syndrome (KOS) (OMIM #608149) is a genetic imprinting disorder affecting chromosome 14 that results in a characteristic phenotype consisting of typical facial features, skeletal abnormalities including rib abnormalities described as “c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc070a1bcd97ff1bad48facd8e51cf67
http://europepmc.org/articles/PMC8159623
http://europepmc.org/articles/PMC8159623
Akademický článek
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