Cryptic mosaicism for monosomy 20 identified in renal tract cells

Clinical Genetics

Volumn 70, Issue 3, 2006, Pages 228-232

  Stefanou, Eunice G ^a   Crocker, M ^b   Boon, A ^c   Stewart, H ^d  

^a UNIVERSITY GENERAL HOSPITAL OF PATRAS   (Greece)

^b Oxford Medical Genetics Labs   (United Kingdom)

^c ROYAL BERKSHIRE HOSPITAL   (United Kingdom)

^d CHURCHILL HOSPITAL   (United Kingdom)

Author keywords

Chromosome 20 mosaicism; FISH; Monosomy 20; Trisomy 20

Indexed keywords

ANEUPLOIDY; ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME 20; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; DISOMY; FACE ASYMMETRY; FACE DYSMORPHIA; FETUS DEVELOPMENT; FLUORESCENCE IN SITU HYBRIDIZATION; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; KARYOTYPE 47,XYY; KIDNEY CELL; MALE; MONOSOMY; MUSCLE HYPOTONIA; ORAL BIOPSY; PERINATAL PERIOD; PHENOTYPE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SKIN FIBROBLAST; TRISOMY; URINALYSIS; VESICOURETERAL REFLUX;

ABNORMALITIES, MULTIPLE; CHROMOSOMES, HUMAN, PAIR 20; CYTOGENETIC ANALYSIS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KIDNEY; MALE; MONOSOMY; MOSAICISM; MOUTH MUCOSA; TRISOMY;

EID: 33747129998     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2006.00652.x     Document Type: Article

References (8)

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