Results 261 to 270 of about 9,055,687 (395)

Equity and social justice perspectives on disability inclusion in healthcare services in Nigeria. [PDF]

Commun Med (Lond)
Azubuike PC, Akinreni T, Adai SG, Ogbonna CK, Abba ME, Udofia MD, Odo OJ, Nwadiche M, Imo UF.   +8 more
europepmc   +1 more source

Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Some 7q31 deletions encompass FOXP2, a gene long associated with speech and language disorders. Intragenic pathogenic FOXP2 variants cause FOXP2‐related speech and language disorder, which has been well characterized in the literature. Conversely, the phenotype associated with 7q31 deletions is neglected.
Lottie D. Morison, Ruth Braden, David J. Amor, Angela T. Morgan   +3 more
wiley   +1 more source

English Language Policy in Thailand

, 2017
W. Baker, Wisut Jarunthawatchai
semanticscholar   +1 more source

Evaluation of Three Large Language Models' Response Performances to Inquiries Regarding Post-Abortion Care in the Context of Chinese Language: A Comparative Analysis. [PDF]

Risk Manag Healthc Policy
Xue D, Liao S.
europepmc   +1 more source

A. Tsui and J. Tollefson (eds): Language Policy, Culture, and Identity in Asian Contexts.

, 2007
Annabelle Mooney
openalex   +1 more source

CLCN4‐Related Neurodevelopmental Condition: Characterization of Speech and Language Abilities

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Speech and language difficulties are a core feature of the CLCN4‐related neurodevelopmental condition, but these have not been well described. Here we systematically phenotype speech and language in 13 participants (10 female, aged 1 year 10 months–41 years 10 months) with pathogenic CLCN4 variants (12 missense de novo, 1 premature stop codon ...
Alexandra Garrett, Vera M. Kalscheuer, Rebeca Ridings Figueroa, Elizabeth E. Palmer, Angela T. Morgan   +4 more
wiley   +1 more source

Midwives' Experiences of Caring for Ukrainian War Refugees: A Qualitative Study. [PDF]

Risk Manag Healthc Policy
Leoniuk K, Sobczak K, Kamińska-Skrzyńska W, Janaszczyk A.   +3 more
europepmc   +1 more source

How to Research Korean Language Use of Overseas Koreans: For the fundamental studies to establish Korean language education policy

, 2007
김호정
openalex   +1 more source

Bilingual children as policy agents: Language policy and education policy in minority language medium Early Childhood Education and Care

, 2017
Mari Bergroth, Åsa Palviainen
semanticscholar   +1 more source

Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim, Kristen N. Lee, Amanda B. Pritchard   +2 more
wiley   +1 more source