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D Lacombe

Showing results (51-60 of 225) with videos related to

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Journal of Medical Genetics|August 1, 1993
Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromesD Lacombe, F Serville, D Marchand, et al.
American Journal of Medical Genetics|September 1, 1992
Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3D Lacombe, R Saura, L Taine, et al.
Bulletin De L'Academie Nationale De Medecine|September 16, 2000
[Williams syndrome (microdeletion 7q11.23), model of behavioral phenotype]J Battin, D Lacombe, L Taine, et al.
Archives Francaises De Pediatrie|June 1, 1988
[Breda virus and hemorrhagic enteropathy. Reminder apropos of 1 case]D Lacombe, F Lamouliatte, C Billeaud, et al.
La Revue De Medecine Interne|January 8, 2011
[Azoospermia as a new feature of Fabry disease]D Lacombe, D P Germain, A Papaxanthos-Roche
Biochimica Et Biophysica Acta. Bioenergetics|May 12, 2018
RAS signalling in energy metabolism and rare human diseasesL Dard, N Bellance, D Lacombe, et al.
European Journal of Pediatrics|August 1, 1995
Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritanceD Lacombe, M A Patton, C Elleau, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literatureD Lacombe, J F Chateil, D Fontan, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Osteoporosis in late-diagnosed adult homocystinuric patientsF Parrot, I Redonnet-Vernhet, D Lacombe, et al.
Revue Neurologique|January 1, 1992
[Neurological, dermatological and biological manifestations of porphyria variegata. A study of 3 families of Italian origin in Marseilles area]R Aquaron, D Lacombe, G C Topi, et al.
Pageof 23

Showing results (51-60 of 225) with videos related to

Sort By:
Pageof 23
Journal of Medical Genetics|August 1, 1993
Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromesD Lacombe, F Serville, D Marchand, et al.
American Journal of Medical Genetics|September 1, 1992
Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3D Lacombe, R Saura, L Taine, et al.
Bulletin De L'Academie Nationale De Medecine|September 16, 2000
[Williams syndrome (microdeletion 7q11.23), model of behavioral phenotype]J Battin, D Lacombe, L Taine, et al.
Archives Francaises De Pediatrie|June 1, 1988
[Breda virus and hemorrhagic enteropathy. Reminder apropos of 1 case]D Lacombe, F Lamouliatte, C Billeaud, et al.
La Revue De Medecine Interne|January 8, 2011
[Azoospermia as a new feature of Fabry disease]D Lacombe, D P Germain, A Papaxanthos-Roche
Biochimica Et Biophysica Acta. Bioenergetics|May 12, 2018
RAS signalling in energy metabolism and rare human diseasesL Dard, N Bellance, D Lacombe, et al.
European Journal of Pediatrics|August 1, 1995
Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritanceD Lacombe, M A Patton, C Elleau, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literatureD Lacombe, J F Chateil, D Fontan, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Osteoporosis in late-diagnosed adult homocystinuric patientsF Parrot, I Redonnet-Vernhet, D Lacombe, et al.
Revue Neurologique|January 1, 1992
[Neurological, dermatological and biological manifestations of porphyria variegata. A study of 3 families of Italian origin in Marseilles area]R Aquaron, D Lacombe, G C Topi, et al.
Pageof 23