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Triploidy 69, XXX in a stillborn girl

Halbrecht, I. ; Komlos, L. ; Shabtay, F. ; Solomon, M. ; Böök, J. A.

Clinical genetics, 1973-01, Vol.4 (3), p.210-212 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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Título:
Triploidy 69, XXX in a stillborn girl
Autor: Halbrecht, I. ; Komlos, L. ; Shabtay, F. ; Solomon, M. ; Böök, J. A.
Assuntos: Adult ; Asthma - drug therapy ; Chromatids ; Chromosome Aberrations ; Chromosomes, Human, 1-3 ; Chromosomes, Human, 13-15 ; Chromosomes, Human, 16-18 ; Chromosomes, Human, 19-20 ; Chromosomes, Human, 21-22 and Y ; Chromosomes, Human, 4-5 ; Chromosomes, Human, 6-12 and X ; Diphenhydramine - therapeutic use ; Ephedrine - therapeutic use ; Female ; Fetal Death ; Heart Septal Defects, Ventricular - genetics ; Humans ; Karyotyping ; Lymphocytes - cytology ; Male ; Phenobarbital - therapeutic use ; Polyploidy ; Pregnancy ; Theophylline - therapeutic use
É parte de: Clinical genetics, 1973-01, Vol.4 (3), p.210-212
Notas: istex:A775E98A4DE4CB0C42057E03D53B745E27822823
ArticleID:CGE210
ark:/67375/WNG-R5FJFRKJ-N
Visiting professor. Institute for Medical Genetics, University of Uppsala, Sweden.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Descrição: Complete triploidy was found in lymphocyte cultures From a stillborn full‐term female infant with a birthweight of 1,000 g. The child had B ventricular septal detect of the heart hut no other macroscopic internal or external malformations. The mother, who had a history of prolonged anti‐asthmatic medication, displayed a high incidence of satellite associations and chromatid breakages in her cultured lymphocytes. The possibility that such changes are instrumental in the formation of triploid zygotes is discussed.
Editor: Oxford, UK: Blackwell Publishing Ltd
Idioma: Inglês

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