Suchergebnisse - "Raza, Muhammad Hashim"

PubPharm (20)

1

A rare missense variant in theATP2C2gene is associated with language impairment and related measures

enthalten in: bioRxiv.org | 2023

von Martinelli, A. | Rice, M. | Talcott, J. | +12

2

Innovative Family-Based Genetically Informed Series of Analyses of Whole-Exome Data Supports Likely Inheritance for Grammar in Children with Specific Language Impairment

enthalten in: Children (Basel, Switzerland) | 2023

von Andres, E. | Earnest, K. | Xuan, H. | +3

3

Receptive vocabulary, memory span, and speech articulation in Pakistani children with developmental language disorders

enthalten in: Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence | 2023

von Hafeez, H. | Yasmin, T. | Raza, M. | +4

ErratumIn: Child Neuropsychol. 2022 Jul 4;:1. - PMID 35786400

4

Genome-wide analysis of runs of homozygosity in Pakistani controls with no history of speech or language-related developmental phenotypes

enthalten in: Annals of human biology | 2023

von Yasmin, T. | Andres, E. | Ashraf, K. | +2

5

Working memory span and receptive vocabulary assessment in Urdu speaking children with speech sound disorder

enthalten in: Acta psychologica | 2022

von Yasmin, T. | Hafeez, H. | Sadia, A. | +4

6

Mutations inZBTB20in individuals with persistent stuttering

enthalten in: bioRxiv.org | 2022

von Frigerio Domingues, C. | Raza, M. | Han, T. | +6

7

Family-Based Whole-Exome Analysis of Specific Language Impairment (SLI) Identifies Rare Variants in BUD13, a Component of the Retention and Splicing (RES) Complex

enthalten in: Brain sciences | 2021

von Andres, E. | Earnest, K. | Zhong, C. | +2

8

Study of rare genetic variants in TM4SF20, NFXL1, CNTNAP2, and ATP2C2 in Pakistani probands and families with language impairment

enthalten in: Meta gene | 2021

von Andres, E. | Neely, H. | Hafeez, H. | +4

9

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures

enthalten in: Human molecular genetics | 2021

von Martinelli, A. | Rice, M. | Talcott, J. | +12

10

Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment

enthalten in: Journal of speech, language, and hearing research : JSLHR | 2020

von Andres, E. | Earnest, K. | Smith, S. | +2