Related Experiment Videos

[Fibroblast growth factor receptors and hereditary abnormalities of bone growth]

J Bonaventure¹, F Rousseau, L Legeai-Mallet

¹Unité de recherche sur les handicaps génétiques de l'enfant, Inserm U 393, Institut Necker, Paris, France.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie

|January 1, 1997

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Spectrum of NSD1 mutations in Sotos and Weaver syndromes.

Journal of medical genetics·2003

[Preimplantation genetic diagnosis and its psychological effects].

Journal de gynecologie, obstetrique et biologie de la reproduction·2003

Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3.

Journal of medical genetics·2003

Prenatal diagnosis of spinal muscular atrophy by genetic analysis of circulating fetal cells.

Lancet (London, England)·2003

Identification of seven novel mutations in the GAN gene.

Human mutation·2003

The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.

Journal of medical genetics·2003

See all related articles