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[Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].

AuthorsG Fioretti, L Pagano, S Renda, B Festa, A Rinaldi, A Celona, C Casullo, M Stabile, M L Cavaliere, V Ventruto
JournalMinerva pediatrica (Minerva Pediatr) Vol. 32 Issue 12 Pg. 807-14 (Jun 30 1980) ISSN: 0026-4946 [Print] Italy
Vernacular TitleRassegna di sette casi di patologia autosomica di più raro riscontro. Trisomia 9p; monosomia 18q; ring 21; trisomia6p; trisomia 2q; traslocazione1;21.
PMID7464734 (Publication Type: Case Reports, English Abstract, Journal Article)
Topics
  • Child, Preschool
  • Chromosome Aberrations (genetics)
  • Chromosome Disorders
  • Chromosome Mapping
  • Chromosomes, Human, 1-3
  • Chromosomes, Human, 16-18
  • Chromosomes, Human, 21-22 and Y
  • Chromosomes, Human, 6-12 and X
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Phenotype
  • Translocation, Genetic
  • Trisomy

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