Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment

Cytogenetic and Genome Research

Volumn 116, Issue 1-2, 2007, Pages 135-140

  Murthy, S K ^a   Nygren, A O H ^b   El Shakankiry, H M ^a   Schouten, J P ^b   Al Khayat, A I ^a   Ridha, A ^c   Al Ali, M T ^a  

^a Al Wasl Hospital   (United Arab Emirates)

^b MRC HOLLAND   (Netherlands)

^c DUBAI HOSPITAL   (United Arab Emirates)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DNA METHYLATION; DNA MICROARRAY; DNA PROBE; FAMILIAL DISEASE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENETIC VARIABILITY; GENOME ANALYSIS; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; KARYOTYPE; MALE; MENTAL DEFICIENCY; NEUROLOGIC DISEASE; PATIENT REFERRAL; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SPEECH DISORDER; VALIDATION STUDY;

ANGELMAN SYNDROME; CHILD, PRESCHOOL; CHROMOSOME MAPPING; DNA METHYLATION; FEMALE; GENE DELETION; GENOMIC IMPRINTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; NERVOUS SYSTEM DISEASES; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDES; PEDIGREE; PRADER-WILLI SYNDROME; SPEECH DISORDERS;

EID: 33846669291     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000097433     Document Type: Article

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