Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four‐member family and an unrelated boy

Autor: Andrea D. Praticò, Piero Pavone, Catia Romano, Giovanni Corsello, Simona Domenica Marino, Martino Ruggieri, Silvia Marino, Raffaele Falsaperla, Agata Polizzi, Enrico Parano, Xena Giada Pappalardo

Publikováno v: Molecular Genetics & Genomic Medicine, Vol 8, Iss 4, Pp n/a-n/a (2020)
MOLECULAR GENETICS & GENOMIC MEDICINE 8 (2020). doi:10.1002/mgg3.1109
info:cnr-pdr/source/autori:Piero Pavone; Martino Ruggieri; Simona D. Marino; Giovanni Corsello; Xena Pappalardo; Agata Polizzi; Enrico Parano; Catia Romano; Silvia Marino; Andrea Domenico Pratico; Raffaele Falsaperla/titolo:Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy/doi:10.1002%2Fmgg3.1109/rivista:MOLECULAR GENETICS & GENOMIC MEDICINE/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:8
Molecular Genetics & Genomic Medicine

Background Deletions in chromosome 15q13 have been reported both in healthy people and individuals with a wide range of behavioral and neuropsychiatric disturbances. Six main breakpoint (BP) subregions (BP1‐BP6) are mapped to the 15q13 region and t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9864cb8496b0d2093efab7e69f6f77c5
https://doaj.org/article/7844a4c3d85e47098a766ef09fd592f5