Terminal deletion of the long arm of chromosome 10

Clinical Genetics

Volumn 65, Issue 4, 2004, Pages 294-298

  Scigliano, S ^a   Gregoire M J ^a   Schmitt, M ^a   Jonveaux, P H ^a   LeHeup, B ^a  

^a HÔPITAL D ENFANTS   (France)

Author keywords

Chromosome 10q; Deletion; Malformation; Megabladder; Mental retardation; Prenatal diagnosis; Urinary tract

Indexed keywords

ARTICLE; BLADDER DISTENSION; CASE REPORT; CHILD; CHROMOSOME 10Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME IDENTIFICATION; CLINICAL FEATURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE 46,XX; KARYOTYPE 46,XY; MONOSOMY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SCORING SYSTEM; URINARY TRACT DISEASE; URINARY TRACT OBSTRUCTION;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 10; FEMALE; HUMANS; INFANT, NEWBORN; MONOSOMY; URETHRA; URINARY BLADDER; URINARY TRACT;

EID: 1842581847     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2004.00218.x     Document Type: Article

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