F. Prieto - Concepedia

Author

F. Prieto

Hospital Universitari i Politècnic La Fe

Also Known As

Agustin Roca, F Prieto, F. Prieto, Felix Prieto, Fernanda Barros Prieto, Félix Prieto, F�lix Prieto

Publications

826

Citations

H-Index

Concepts

All Affiliations

Hospital Universitari i Politècnic La Fe Universitat de València Instituto de Investigación Sanitaria La Fe

About

F. Prieto is an author at Hospital Universitari i Politècnic La Fe specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	263
2	Molecular Biology	2	2	189
3	Natural Sciences	1	1	16
4	Public Health	1	1	173
5	Biology	1	1	16

F. Prieto

Publications

628

Citations

H-Index

Page 1

	Year	Citations
Phenotype Correlation and Intergenerational Dynamics of the Friedreich Ataxia GAA Trinucleotide Repeat Eugènia Monrós, María Dolores Moltó, Francisco Martı́nez, The American Journal of Human Genetics Genetic AnalysisGenetic DisorderGeneticsGenetic EpidemiologyMolecular Biology	1997	173
Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome Oliver Bartsch, Ulrich K�nig, Michael B. Petersen, Human Genetics	1993	77
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes Françesc Solé, F. Prieto, S Woessner, Cancer Genetics and Cytogenetics Hematological MalignancyHematologyPathologyAneuploidyCytogenetic Studies	1992	63
Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features Carmen Orellana, JM Millán, MR Montero, Clinical Genetics	2001	45
Heart-hand syndrome Salvador Ruiz de la Fuente, F. Prieto Human Genetics	1980	36
Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin–Lowry syndrome Isabel Martínez‐Garay, MJ Ballesta, Silvestre Oltra, Clinical Genetics	2003	32
X‐linked dysmorphic syndrome with mental retardation F. Prieto, Fernando Mulas, Francisco J. Caballero Mora Clinical Genetics	1987	27
10p- Syndrome associated with multiple chromosomal abnormalities F. Prieto, J. A. Moreno, P. Barbero, Human Genetics Down SyndromeCytogeneticsGenetic DisorderGeneticsPathology	1978	25
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR Rebeca Valero, Gemma Marfany, Rosario Gil‐Benso, Journal of Medical Genetics	1999	25
Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers. Marta Tomàs, José M. Millán, Ana I. Fernández, Journal of Medical Genetics Developmental AnomalyX InactivationSevere Mental RetardationDevelopmental BiologyMendelian Disorder	1998	22

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