American Journal of Medical Genetics · 1996 · 13 citations · 7 references
Life SciencesGeneticsPediatricsCytogeneticsHuman GeneticsPediatric GeneticsChromosomal AbnormalitiesChromosomal DisordersCongenital Craniofacial AnomaliesCraniofacial AnomaliesMosaicismNumerical Chromosome AbnormalitiesAssociated Craniofacial AnomaliesAutosomal TrisomyComparative Clinical ManifestationsCongenital Craniofacial Anomalies GeneticsCraniofacial Developmental AnomaliesMosaic TrisomySyndromic Craniofacial AnomaliesSyndromic Craniofacial Disorders
We report on a boy with mosaic trisomy 15. The clinical manifestations are compared with those of the few cases reported up to now. A clinical syndrome is delineated consisting of a characteristic shape of the nose and other minor craniofacial anomalies, as well as typical deformities of the hands and feet. Different degrees of mosaicism may explain the more or less severe manifestations in individual patients.
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Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.
Elisabeth Blennow, H. Telenius, Diana de Vos et al. · PubMed · 1994 · 80 citations
A case of trisomy of chromosome 15
S Coldwell, B Fitzgerald, J M Semmens et al. · Journal of Medical Genetics · 1981 · 37 citations · Full text
Life Sciences, Genetics, Pediatrics +14
Distal 15q trisomy: phenotypic comparison of nine cases in an extended family.
P Schnatterly, K L Bono, Meinhard Robinow et al. · PubMed · 1984 · 25 citations