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L Taine

Showing results (1-10 of 41) with videos related to

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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.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 26, 1999
A YAC contig encompassing the 11q14.3 breakpoint of a translocation associated with schizophrenia, and including the tyrosinase geneJ Petit, P Boisseau, L Taine, et al.
Lancet (London, England)|May 21, 1998
Safety and fetal outcome of early and midtrimester amniocentesisR Saura, L Taine, F Guyon, et al.
Prenatal Diagnosis|September 1, 1994
Amniotic fluid leakage and miscarriages after TA-CVSR Saura, L Taine, Z Q Wen, et al.
Human Genetics|April 1, 1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33L Taine, I Coupry, P Boisseau, et al.
Revue De Laryngologie - Otologie - Rhinologie|January 1, 1997
[ORL and speech aspects in DiGeorge syndrome]D Portmann, M Marraco, D Lacombe, et al.
Cancer Genetics and Cytogenetics|May 1, 1992
A simple method of chromosomal analysis for malignant solid tumorsR Saura, O Grison, L Taine, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Trisomy 22 with thyroid isthmus agenesis and absent gall bladderE Gangbo, D Lacombe, E M Alberti, et al.
Prenatal Diagnosis|January 1, 1994
Is non-echogenic nuchal oedema a marker in trisomy 21 screening?R Saura, J L Brun, L Taine, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
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.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 26, 1999
A YAC contig encompassing the 11q14.3 breakpoint of a translocation associated with schizophrenia, and including the tyrosinase geneJ Petit, P Boisseau, L Taine, et al.
Lancet (London, England)|May 21, 1998
Safety and fetal outcome of early and midtrimester amniocentesisR Saura, L Taine, F Guyon, et al.
Prenatal Diagnosis|September 1, 1994
Amniotic fluid leakage and miscarriages after TA-CVSR Saura, L Taine, Z Q Wen, et al.
Human Genetics|April 1, 1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33L Taine, I Coupry, P Boisseau, et al.
Revue De Laryngologie - Otologie - Rhinologie|January 1, 1997
[ORL and speech aspects in DiGeorge syndrome]D Portmann, M Marraco, D Lacombe, et al.
Cancer Genetics and Cytogenetics|May 1, 1992
A simple method of chromosomal analysis for malignant solid tumorsR Saura, O Grison, L Taine, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Trisomy 22 with thyroid isthmus agenesis and absent gall bladderE Gangbo, D Lacombe, E M Alberti, et al.
Prenatal Diagnosis|January 1, 1994
Is non-echogenic nuchal oedema a marker in trisomy 21 screening?R Saura, J L Brun, L Taine, et al.
Pageof 5