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Volumn 110, Issue 1, 2002, Pages 73-77
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Terminal deletion of the chromosome 7(q36-qter) in an infant with sacral agenesis and anterior myelomeningocele
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Author keywords
Chromosome 7; Chromosome deletion; FISH; Sacral agenesis
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Indexed keywords
ARTICLE;
CAFE AU LAIT SPOT;
CASE REPORT;
CHROMOSOME 7Q;
CHROMOSOME ANALYSIS;
CHROMOSOME DELETION;
CHROMOSOME DELETION 7Q;
COLOBOMA;
FACE MALFORMATION;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENE LOCATION;
HAPLOTYPE;
HOMEOBOX;
HUMAN;
MALE;
MENINGOMYELOCELE;
MENTAL DEFICIENCY;
MICROCEPHALY;
PARTIAL MONOSOMY;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
SACRUM AGENESIS;
CHROMOSOME BANDING;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 7;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
INFANT;
MALE;
MENINGOMYELOCELE;
SACRUM;
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EID: 0036605109
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/ajmg.10365 Document Type: Article |
Times cited : (24)
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References (19)
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