A unique de novo interstitial deletion del(17) (q21.3q23) in a phenotypically abnormal infant
- Author
- PARK, J. P1 ; MOESCHLER, J. B; BERG, S. Z; BAUER, R. M; WURSTER-HILL, D. H
[1] Dartmouth coll., child development cent., dep. patholoy clin. genetics, Hanover NH 03756, United States - Source
Clinical genetics. 1992, Vol 41, Num 1, pp 54-56
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Chromosome E17 anormal De novo Délétion Etude cas Nourrisson Phénotype Aberration chromosomique Chromosome anormal Homme
- Keyword (en)
- Abnormal E17 chromosome De novo Deletion Case study Infant Phenotype Chromosomal aberration Abnormal chromosome Human
- Keyword (es)
- Cromosoma E17 anormal De novo Deleción Estudio caso Lactante Fenotipo Aberración cromosómica Cromosoma anormal Hombre
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23B Chromosome aberrations
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5169087
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
10.1111/j.1399-0004.1992.tb03631.x 
https://dx.doi.org/10.1111/j.1399-0004.1992.tb03631.x
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