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American Journal of Medical Genetics
|
September 1, 1992
Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3
D 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 gene
J Petit, P Boisseau, L Taine, et al.
Lancet (London, England)
|
May 21, 1998
Safety and fetal outcome of early and midtrimester amniocentesis
R Saura, L Taine, F Guyon, et al.
Prenatal Diagnosis
|
September 1, 1994
Amniotic fluid leakage and miscarriages after TA-CVS
R Saura, L Taine, Z Q Wen, et al.
Human Genetics
|
April 1, 1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33
L 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 tumors
R Saura, O Grison, L Taine, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
Trisomy 22 with thyroid isthmus agenesis and absent gall bladder
E 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.
Page
of 5
Search research articles
Search
Showing results (1-10 of 41) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics
|
September 1, 1992
Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3
D 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 gene
J Petit, P Boisseau, L Taine, et al.
Lancet (London, England)
|
May 21, 1998
Safety and fetal outcome of early and midtrimester amniocentesis
R Saura, L Taine, F Guyon, et al.
Prenatal Diagnosis
|
September 1, 1994
Amniotic fluid leakage and miscarriages after TA-CVS
R Saura, L Taine, Z Q Wen, et al.
Human Genetics
|
April 1, 1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33
L 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 tumors
R Saura, O Grison, L Taine, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
Trisomy 22 with thyroid isthmus agenesis and absent gall bladder
E 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.
Page
of 5