Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia-Reference-Cited by-同舟云学术

Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia

Published:2006-11 Issue:5 Volume:79 Page:965-972
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Feuk Lars,Kalervo Aino,Lipsanen-Nyman Marita,Skaug Jennifer,Nakabayashi Kazuhiko,Finucane Brenda,Hartung Danielle,Innes Micheil,Kerem Batsheva,Nowaczyk Małgorzata J.,Rivlin Joseph,Roberts Wendy,Senman Lili,Summers Anne,Szatmari Peter,Wong Virginia,Vincent John B.,Zeesman Susan,Osborne Lucy R.,Cardy Janis Oram,Kere Juha,Scherer Stephen W.,Hannula-Jouppi Katariina

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference34 articles.

1. The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder;Lai;Am J Hum Genet,2000

2. A forkhead-domain gene is mutated in a severe speech and language disorder;Lai;Nature,2001

3. An extended family with a dominantly inherited speech disorder;Hurst;Dev Med Child Neurol,1990

4. Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene;Shu;Proc Natl Acad Sci USA,2005

5. FOXP2: novel exons, splice variants, and CAG repeat length stability;Bruce;Hum Genet,2002

Cited by 153 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Childhood Apraxia of Speech: A Descriptive and Prescriptive Model of Assessment and Diagnosis;Brain Sciences;2024-05-24

2. Unraveling the interplay between the leucine zipper and forkhead domains of FOXP2: Implications for DNA binding, stability and dynamics;Proteins: Structure, Function, and Bioinformatics;2024-05-15

3. Case report: Paternal uniparental disomy on chromosome 7 and homozygous SUGCT mutation in a fetus with overweight after birth;Frontiers in Genetics;2023-10-17

4. Clinical and Molecular Heterogeneity of Silver-Russell Syndrome and Therapeutic Challenges: A Systematic Review;Current Pediatric Reviews;2023-05

5. Executive functioning in adolescents and adults with Silver-Russell syndrome;PLOS ONE;2023-01-20