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Search Results - Le Fevre, Anna K.
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FOXP1 mutations cause intellectual disability and a recognizable phenotype
by
Le Fevre, Anna K.
,
Taylor, Sharelle
,
Malek, Neva H.
,
Horn, Denise
,
Carr, Christopher W.
,
Abdul-Rahman, Omar A.
,
O'Donnell, Sherindan
,
Burgess, Trent
,
Shaw, Marie
,
Gecz, Jozef
,
Bain, Nicole
,
Fagan, Kerry
,
Hunter, Matthew F.
Published in
American journal of medical genetics. Part A
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American Journal Of Medical Genetics Part A
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American Journal Of Medical Genetics. Part A
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3P13
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Animals
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Autism
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Autistic Disorder - Genetics
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Autistic Disorder - Physiopathology
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Child
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Chromosomal Microdeletion
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Congenital Defects
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Developmental Disabilities - Genetics
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Developmental Disabilities - Physiopathology
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Fetuses
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Forkhead Transcription Factors - Genetics
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Foxp1
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Foxp1 Protein
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Foxp2 Protein
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Genetics & Heredity
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Haploinsufficiency
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Haploinsufficiency - Genetics
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Humans
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Intellectual Disabilities
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