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S Lyonnet

Showing results (61-70 of 223) with videos related to

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European Journal of Human Genetics : EJHG|August 31, 2001
TP63 gene mutation in ADULT syndromeJ Amiel, G Bougeard, C Francannet, et al.
Prenatal Diagnosis|May 1, 1994
Prenatal diagnosis of combined methylmalonic aciduria and homocystinuria (cobalamin CblC or CblD mutant)B Chadefaux-Vekemans, M O Rolland, S Lyonnet, et al.
Lancet (London, England)|December 24, 1994
De-novo mutations of the RET proto-oncogene in Hirschsprung's diseaseA Pelet, T Attie, O Goulet, et al.
European Journal of Pediatrics|July 1, 1992
X-linked hydrocephalus: clinical heterogeneity at a single gene locusF Serville, S Lyonnet, A Pelet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1995
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]D Bonnet, J Terrett, E Pequignot-Viegas, et al.
Journal of Medical Genetics|April 1, 1995
Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Contribution of genetics]S Lyonnet, N Morichon, M Dommergues, et al.
Prenatal Diagnosis|March 1, 2000
Dicentric marker derived from chromosome 22 associated with mild clinical signs: a case reportL Lohmann, N Chelloug, B Rosales, et al.
American Journal of Medical Genetics|August 15, 1994
Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndromeP Edery, Y Manach, M Le Merrer, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 3, 2015
[Kabuki syndrome: Update and review]M Arnaud, M Barat-Houari, V Gatinois, et al.
Pageof 23

Showing results (61-70 of 223) with videos related to

Sort By:
Pageof 23
European Journal of Human Genetics : EJHG|August 31, 2001
TP63 gene mutation in ADULT syndromeJ Amiel, G Bougeard, C Francannet, et al.
Prenatal Diagnosis|May 1, 1994
Prenatal diagnosis of combined methylmalonic aciduria and homocystinuria (cobalamin CblC or CblD mutant)B Chadefaux-Vekemans, M O Rolland, S Lyonnet, et al.
Lancet (London, England)|December 24, 1994
De-novo mutations of the RET proto-oncogene in Hirschsprung's diseaseA Pelet, T Attie, O Goulet, et al.
European Journal of Pediatrics|July 1, 1992
X-linked hydrocephalus: clinical heterogeneity at a single gene locusF Serville, S Lyonnet, A Pelet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1995
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]D Bonnet, J Terrett, E Pequignot-Viegas, et al.
Journal of Medical Genetics|April 1, 1995
Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Contribution of genetics]S Lyonnet, N Morichon, M Dommergues, et al.
Prenatal Diagnosis|March 1, 2000
Dicentric marker derived from chromosome 22 associated with mild clinical signs: a case reportL Lohmann, N Chelloug, B Rosales, et al.
American Journal of Medical Genetics|August 15, 1994
Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndromeP Edery, Y Manach, M Le Merrer, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 3, 2015
[Kabuki syndrome: Update and review]M Arnaud, M Barat-Houari, V Gatinois, et al.
Pageof 23