Pure distal 9p deletion in a female infant with cerebral palsy

Genetic Counseling

Volumn 23, Issue 2, 2012, Pages 215-221

  Chen, Chih Ping ^a,b,c,d,e   Lin, S P ^a,f   Su, Y N ^g   Su, J W ^a,h   Chern, S R ^a   Town, D D ^a   Wang, W ^a,i  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b ASIA UNIVERSITY   (Taiwan)

^c CHINA MEDICAL UNIVERSITY   (Taiwan)

^d NATIONAL YANG MING UNIVERSITY   (Taiwan)

^e MACKAY MEDICAL COLLEGE   (Taiwan)

^f NURSING AND MANAGEMENT COLLEGE   (Taiwan)

^g NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^h CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

ⁱ TATUNG UNIVERSITY   (Taiwan)

Author keywords

9p deletion syndrome; ANKRD15; Cerebral palsy; DOCK8; FOXD4; Monosomy 9p; VLDLR

Indexed keywords

ARTICLE; BRAIN DYSFUNCTION; CASE REPORT; CEREBRAL PALSY; CHROMOSOME 9P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DELETION 9P; DEVELOPMENTAL DISORDER; DNA MARKER; ELECTROENCEPHALOGRAPHY; FEMALE; GENE; GENOTYPE; HUMAN; HYPOPLASIA; INFANT; MENTAL DEFICIENCY; MUSCLE HYPOTONIA; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; SPEECH DISORDER;

ABNORMALITIES, MULTIPLE; CEREBRAL PALSY; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GUANINE NUCLEOTIDE EXCHANGE FACTORS; HUMANS; INFANT; RECEPTORS, LDL; TUMOR SUPPRESSOR PROTEINS;

EID: 84864446708     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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