Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies.

Bhat, S S; Schmidt, K R; Ladd, S; Kim, K C; Schwartz, C E; Simensen, R J; DuPont, B R; Stevenson, R E; Srivastava, A K

Bhat, S S; Schmidt, K R; Ladd, S; Kim, K C; Schwartz, C E; Simensen, R J; DuPont, B R; Stevenson, R E; Srivastava, A K.

Affiliation

Bhat SS; J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, SC, USA.

Cytogenet Genome Res ; 112(1-2): 170-5, 2006.

Article in En | MEDLINE | ID: mdl-16276108

Subject(s)

Abnormalities, Multiple/genetics; Coenzyme A Ligases/genetics; Developmental Disabilities/genetics; Dystrophin/genetics; Intellectual Disability/genetics; Muscle Hypotonia/genetics; Birth Weight; Child; Chromosome Aberrations; Chromosomes, Human, X; Female; Humans; Infant, Newborn; Male; Sequence Deletion

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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Developmental Disabilities / Dystrophin / Coenzyme A Ligases / Intellectual Disability / Muscle Hypotonia Limits: Child / Female / Humans / Male / Newborn Language: En Journal: Cytogenet Genome Res Journal subject: GENETICA Year: 2006 Type: Article Affiliation country: United States

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