Prenatal diagnosis of monosomy 1p36: A focus on brain abnormalities and a review of the literature

American Journal of Medical Genetics, Part A

Volumn 146, Issue 23, 2008, Pages 3062-3069

  Campeau, Philippe M ^a   Mew, Nicholas Ah ^a   Cartier, Lola ^a   Mackay, Katherine L ^b   Shaffer, Lisa G ^b,c   Der Kaloustian, Vazken M ^a   Thomas, Mary Ann ^d,e  

^a MCGILL UNIVERSITY   (Canada)

^b WASHINGTON STATE UNIVERSITY   (United States)

^c PerkinElmer   (United States)

^d UNIVERSITY OF CALGARY   (Canada)

^e ALBERTA CHILDREN'S HOSPITAL   (Canada)

Author keywords

1p36; Array sequence analysis; Cerebral ventricles; Chromosome 1; Chromosome 20; Fluorescence; Hydrocephalus; In situ hybridization; Oligonucleotide; Polymicrogyria; Prenatal diagnosis; Terminal deletion

Indexed keywords

AMNIOCENTESIS; ANAMNESIS; ARTICLE; AUTOPSY; BRAIN DISEASE; CASE REPORT; CHROMOSOME 1P; CHROMOSOME DELETION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; HOLOPROSENCEPHALY; HUMAN; HYDROCEPHALUS; INFANT; KARYOTYPE; MONOSOMY; MYELINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PERINATAL PERIOD; PRENATAL DIAGNOSIS; PRENATAL PERIOD; PRIORITY JOURNAL; TRISOMY; ULTRASOUND;

BRAIN; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; FETUS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MONOSOMY; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PREGNANCY; PRENATAL DIAGNOSIS; ULTRASONOGRAPHY, PRENATAL;

EID: 57149108008     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32563     Document Type: Article

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