Deletion 22q13.3 syndrome.

Phelan, Mary C

Phelan, Mary C.

Affiliation

Phelan MC; Cytogenetics Laboratory, Molecular Pathology Laboratory Network, 250 East Broadway, Maryville, TN 37804, USA. kphelan@mplnet.com

Orphanet J Rare Dis ; 3: 14, 2008 May 27.

Article in En | MEDLINE | ID: mdl-18505557

Subject(s)

Chromosome Deletion; Chromosomes, Human, Pair 22; Developmental Disabilities/genetics; Speech Disorders/genetics; Carrier Proteins/genetics; Child; Diagnosis, Differential; Genetic Counseling; Humans; In Situ Hybridization, Fluorescence; Nerve Tissue Proteins; Prenatal Diagnosis; Prognosis; Syndrome

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Speech Disorders / Chromosomes, Human, Pair 22 / Developmental Disabilities / Chromosome Deletion Type of study: Diagnostic_studies / Prognostic_studies Limits: Child / Humans Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2008 Type: Article Affiliation country: United States

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