Journal of Medical Genetics · 1995 · 53 citations · 1 references
Life SciencesGeneticsMolecular GeneticsCytogeneticsHuman GeneticsMedical GeneticsChromosomal AbnormalitiesChromosomal DisordersGenetic DisordersMolecular CytogeneticsPrenatal CytogeneticsStructural Chromosome AbnormalitiesChromosomal DeletionsChromosome DeletionsGene Deletion SyndromesMicrodeletion SyndromesPrenatal Chromosomal DiagnosisPrenatal Cytogenetic DiagnosisPrenatal Molecular DiagnosisTerminal Deletions
A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother. The deletion was confirmed by FISH. The breakpoint is distal to the region responsible for the 3p- syndrome. A normal baby girl was born with no apparent phenotypic abnormalities.
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Molecular genetic analysis of the 3p — syndrome
Maude E. Phipps, Farida Latif, Amanda Prowse et al. · Human Molecular Genetics · 1994 · 45 citations · Full text