Výsledky vyhledávání - "ND Vashkamadze"

P79 Clinical case of rare chromosome pathology: combined deletion 7p21.1-p15.2 and deletion 22q12.1 in patient with mental retardation

Autor: AA Pushkov, L.S. Namazova-Baranova, Natalya Zhurkova, ND Vashkamadze, TA Polunina, Kirill Savostyanov

Publikováno v: Posters.

Background and aims Last five years more than 50 novel microdeletion and microduplication syndromes were described. Sometimes we find rare chromosome anomalies, which clinical significance is not always known. Our aim was to describe the new phenotyp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b29bf24d1397dda43469ca4b76a7d804
https://doi.org/10.1136/archdischild-2017-313273.167

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání