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Showing results (101-110 of 223) with videos related to

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Journal of Medical Genetics|September 22, 2001
GDNF as a candidate modifier in a type 1 neurofibromatosis (NF1) enteric phenotypeM Bahuau, A Pelet, D Vidaud, et al.
Human Genetics|November 1, 1994
A novel polymorphism in the coding sequence of the human RET proto-oncogeneP Edery, T Attié, L M Mulligan, et al.
Prenatal Diagnosis|June 1, 1993
Prenatal exclusion of X-linked hydrocephalus-stenosis of the aqueduct of Sylvius sequence using closely linked DNA markersF Serville, P Benit, P Saugier, et al.
Heart (British Cardiac Society)|April 16, 1998
Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defectM Chessa, G Butera, P Bonhoeffer, et al.
Journal of Medical Genetics|April 16, 1999
Investigation of germline GFR alpha-1 mutations in Hirschsprung diseaseS M Myers, R Salomon, A Goessling, et al.
European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.
Annales De Chirurgie|January 1, 1996
[Genetics of Hirschsprung disease]T Attié, J Amiel, D Jan, et al.
Journal of Medical Genetics|October 1, 1992
The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24)M Le Merrer, K Ben Othmane, V Stanescu, et al.
The British Journal of Dermatology|August 1, 1994
Disseminated superficial porokeratosis in a patient with AIDSJ Kanitakis, L Misery, J F Nicolas, et al.
Clinical Genetics|April 14, 2015
A review of craniofacial disorders caused by spliceosomal defectsD Lehalle, D Wieczorek, R M Zechi-Ceide, et al.
Pageof 23

Showing results (101-110 of 223) with videos related to

Sort By:
Pageof 23
Journal of Medical Genetics|September 22, 2001
GDNF as a candidate modifier in a type 1 neurofibromatosis (NF1) enteric phenotypeM Bahuau, A Pelet, D Vidaud, et al.
Human Genetics|November 1, 1994
A novel polymorphism in the coding sequence of the human RET proto-oncogeneP Edery, T Attié, L M Mulligan, et al.
Prenatal Diagnosis|June 1, 1993
Prenatal exclusion of X-linked hydrocephalus-stenosis of the aqueduct of Sylvius sequence using closely linked DNA markersF Serville, P Benit, P Saugier, et al.
Heart (British Cardiac Society)|April 16, 1998
Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defectM Chessa, G Butera, P Bonhoeffer, et al.
Journal of Medical Genetics|April 16, 1999
Investigation of germline GFR alpha-1 mutations in Hirschsprung diseaseS M Myers, R Salomon, A Goessling, et al.
European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.
Annales De Chirurgie|January 1, 1996
[Genetics of Hirschsprung disease]T Attié, J Amiel, D Jan, et al.
Journal of Medical Genetics|October 1, 1992
The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24)M Le Merrer, K Ben Othmane, V Stanescu, et al.
The British Journal of Dermatology|August 1, 1994
Disseminated superficial porokeratosis in a patient with AIDSJ Kanitakis, L Misery, J F Nicolas, et al.
Clinical Genetics|April 14, 2015
A review of craniofacial disorders caused by spliceosomal defectsD Lehalle, D Wieczorek, R M Zechi-Ceide, et al.
Pageof 23