J. F. Mattéi - Concepedia

Author

J. F. Mattéi

Also Known As

J F Mattei, J F Mattéi, J MATTEI, J. -F. Mattei, J. F. MATTEI, J. F. Mattei, J. F. Mattéi, J.-F. Mattei, J.-F. Mattéi, J.-Fr. Mattei

114

Publications

3.5K

Citations

H-Index

115

Concepts

All Affiliations

Hôpital d'Enfants Hôpital de la Timone Inserm Centre National de la Recherche Scientifique Université Paris Cité

About

J. F. Mattéi is an author at Hôpital d'Enfants specializing in medicine, genetics, and cytogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	48	2.8K
2	Natural Sciences	4	4	402
3	Health Sciences	2	2	79
4	Education	1	1	74
5	Engineering	1	1	70

J. F. Mattéi

Publications

3.1K

Citations

H-Index

Page 1

	Year	Citations
DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome Marie‐Geneviève Mattéi, N. Philip, E. Passage, Human Genetics BiologyChromatinDna SequencingDnaCytogenetics	1985	313
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome. Zohra Rahmani, Jean‐Louis Blouin, N. Créau-Goldberg, Proceedings of the National Academy of Sciences Down SyndromeChromatinD21s55 RegionPartial DuplicationDevelopmental Biology	1989	260
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male Giovanna Camerino, Marie‐Geneviève Mattéi, J. F. Mattéi, Nature Close LinkageGenetic DisorderGeneticsFragile X SpectrumMedicine	1983	167
X-Autosome translocations: Cytogenetic characteristics and their consequences Marie‐Geneviève Mattéi, J. F. Mattéi, Ségolène Aymé, Human Genetics ChromatinX-autosome TranslocationsCytogeneticsGeneticsChromosome Biology	1982	155
The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice A. Dautigny, Marie‐Geneviève Mattéi, D. Morello, Nature Knockout MouseMolecular NeuroscienceDevelopmental BiologySignal TransductionStructural Gene	1986	154
Constitutional chromosomal breakage F Giraud, Ségolène Aymé, J. F. Mattéi, Human Genetics Constitutional Chromosomal BreakageGeneticsChromosome BiologyChromosomal RearrangementMedicine	1976	147
Mapping of the human retinoic acid receptor to the q21 band of chromosome 17 Marie‐Geneviève Mattéi, Martin Petkovich, J. F. Mattéi, Human Genetics ChromatinSignal TransductionCytogeneticsGeneticsReceptor (Biochemistry)	1988	112
Prader-Willi syndrome and chromosome 15 J. F. Mattéi, Marie‐Geneviève Mattéi, F Giraud Human Genetics Chromosome 15Mendelian DisorderGenetic DisorderGeneticsPathology	1983	86
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach Marie‐Geneviève Mattéi, J. F. Mattéi, Isabel Ferreirós-Vidal, Human Genetics ChromatinCytogeneticsLymphocyte DevelopmentImmunologyFragile X Spectrum	1981	82
Structural anomalies of the X chromosome and inactivation center Marie‐Geneviève Mattéi, J. F. Mattéi, Isabel Ferreirós-Vidal, Human Genetics ChromatinChromatin StructureCytogeneticsGeneticsChromosome Biology	1981	82

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