An analysis of Xq deletions
- Author
- MARASCHIO, P1 ; TUPLER, R1 ; BARBIERATO, L1 ; DAINOTTI, E1 ; LARIZZA, D; BERNARDI, F; HOELLER, H; GARAU, A; TIEPOLO, L1
[1] Univ. Pavia, biologia gen. genetica medica, 27100 Pavia, Italy - Source
Human genetics. 1996, Vol 97, Num 3, pp 375-381 ; ref : 26 ref
- CODEN
- HUGEDQ
- ISSN
- 0340-6717
- Scientific domain
- Biotechnology; Genetics
- Publisher
- Springer, Berlin
/
Springer, Heidelberg
/
Springer, New York, NY
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Chromosome X anormal Cytogénétique Délétion Homme Monosomie Mosaïcisme Phénotype Aberration chromosomique Aneuploïdie Chromosome anormal
- Keyword (en)
- Abnormal X chromosome Cytogenetics Deletion Human Monosomy Mosaicism Phenotype Chromosomal aberration Aneuploidy Abnormal chromosome
- Keyword (es)
- Cromosoma X anormal Citogenética Deleción Hombre Monosomía Mosaicismo Fenotipo Aberración cromosómica Aneuploidía Cromosoma anormal
- 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
- 2975379
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
10.1007/BF02185777 
https://dx.doi.org/10.1007/BF02185777
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