Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin-neurexin hypothesis

Autism, language and communication in children with sex chromosome trisomies

(2010) D. V. M. Bishop et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Overlaps Between Autism and Language Impairment: Phenomimicry or Shared Etiology?

(2010) D. V. M. Bishop   BEHAVIOR GENETICS

CAUSES AND ASSOCIATIONS OF SEVERE AND PERSISTENT SPECIFIC SPEECH AND LANGUAGE DISORDERS IN CHILDREN

(2010) Roger J. Robinson   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review*

(2010) VICTORIA LEGGETT et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

An extra X or Y chromosome: Contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome

(2009) Judith L. Ross et al.   Developmental Disabilities Research Reviews

Psychiatric Characteristics in a Self-Selected Sample of Boys With Klinefelter Syndrome

(2009) H. Bruining et al.   PEDIATRICS

Cognitive and motor development during childhood in boys with Klinefelter syndrome

(2008) Judith L. Ross et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

No evidence for involvement of genetic variants in the X-linked neuroligin genesNLGN3andNLGN4Xin probands with autism spectrum disorder on high functioning level

(2008) Anne-Kathrin Wermter et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Failure of neuronal homeostasis results in common neuropsychiatric phenotypes

(2008) Melissa B. Ramocki et al.   NATURE

Advances in autism genetics: on the threshold of a new neurobiology

(2008) Brett S. Abrahams et al.   NATURE REVIEWS GENETICS

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE