Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques
- Author
- QUMSIYEH, M. B1 ; TOMASI, A; TASLIMI, M
[1] Duke univ. medical cent., cytogenetics lab., Durham NC 27710, United States - Source
Journal of medical genetics. 1995, Vol 32, Num 12, pp 991-993 ; ref : 27 ref
- Publisher
- BMJ, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Chromosome E18 anormal Diagnostic Délétion Foetus pathologie Homme Isochromosome Mosaïcisme Prénatal Aberration chromosomique Chromosome anormal Gestation pathologie
- Keyword (en)
- Abnormal chromosome E18 Diagnosis Deletion Fetal diseases Human Isochromosome Mosaicism Prenatal Chromosomal aberration Abnormal chromosome Pregnancy disorders
- Keyword (es)
- Cromosoma E18 anormal Diagnóstico Deleción Feto patología Hombre Isocromosoma Mosaicismo Prenatal Aberración cromosómica Cromosoma anormal Gestación patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B20 Gynecology. Andrology. Obstetrics / 002B20F Pregnancy. Fetus. Placenta / 002B20F01 Management. Prenatal diagnosis
- Discipline
- Gynecology. Andrology. Obstetrics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2940863
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1136/jmg.32.12.991 
https://dx.doi.org/10.1136/jmg.32.12.991
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