F Chavin-Colin - Concepedia

Author

F Chavin-Colin

Hôpital Necker-Enfants Malades

Also Known As

F Chavin-Colin, F. Chavin-Colin, F. Chavin‐Colin, Françoise Chavin-Colin, Fran�oise Chavin-Colin

Publications

759

Citations

H-Index

Concepts

All Affiliations

Hôpital Necker-Enfants Malades Hôpital des Enfants Centre National de la Recherche Scientifique Inserm Sorbonne Université

About

F Chavin-Colin is an author at Hôpital Necker-Enfants Malades specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	348
2	Pathology	3	3	167
3	Molecular Genetics	2	2	62
4	Cell Biology	1	1	44
5	Nephrology	1	1	54

F Chavin-Colin

Publications

647

Citations

H-Index

Page 1

	Year	Citations
Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases C Turleau, J. de Grouchy, F Chavin-Colin, Human Genetics Beckwith-wiedemann SyndromeMendelian DisorderCongenital DisordersGenetic Disorder	1984	156
Cytogenetic forms of retinoblastoma: Their incidence in a survey of 66 patients C Turleau, J. de Grouchy, F Chavin-Colin, Cancer Genetics and Cytogenetics Cytogenetic FormsMedicinePathologyOphthalmology	1985	69
Partial trisomy 9q: A new syndrome C Turleau, J. de Grouchy, F Chavin-Colin, Human Genetics Down SyndromePartial Trisomy 9QGenetic DisorderGeneticsMedicine	1975	64
Cytogenetic investigation in 413 couples with spontaneous abortions C Turleau, F Chavin-Colin, J. de Grouchy European Journal of Obstetrics & Gynecology and Reproductive Biology InfertilityFertilityAbortionCytogeneticsGenetics	1979	55
Del11p13/nephroblastoma without aniridia C Turleau, J. de Grouchy, Claire Nihoul‐Feketé, Human Genetics UrologyMedicineKidney FailureRenal PathologySurgical Pathology	1984	54
Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8 J. de Grouchy, Marie‐Dominique Dautzenberg, C Turleau, Human Genetics ThrombosisHematologyChromosome 8PathologyHemostasis	1984	44
Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin). C Turleau, de Grouchy J, F Chavin-Colin, PubMed	1984	43
Trisomy 18q‐. Trisomy mapping of chromosome 18 revisited C Turleau, F Chavin-Colin, R Narbouton, Clinical Genetics	1980	40
Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers C Turleau, F Chavin-Colin, J. de Grouchy, Human Genetics Familial TCytogeneticsGenetic DisorderGeneticsGenetic Epidemiology	1977	36
A 45,X male with translocation of euchromatic Y chromosome material C Turleau, F Chavin-Colin, J. de Grouchy Human Genetics CytogeneticsGenetic DisorderGeneticsChromosome BiologyMolecular Genetics	1980	26

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