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Journal of Medical Genetics
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August 4, 2025
Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with <i>NF1</i> point variants
Laurence Pacot, Marinus Blok, Dominique Vidaud, et al.
Cancer Discovery
|
April 10, 2022
PD-1 Blockade in Solid Tumors with Defects in Polymerase Epsilon
Benoit Rousseau, Ivan Bieche, Eric Pasmant, et al.
Annales D'Endocrinologie
|
March 21, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions
Laurence Faivre, Camille Level, Régis Coutant, et al.
Annales D'Endocrinologie
|
May 8, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions
Laurence Faivre, Camille Level, Régis Coutant, et al.
Page
of 13
Search research articles
Search
Showing results (121-130 of 124) with videos related to
Sort By:
Page
of 13
You have reached the last page of results.
This site can display upto 124 results.
Journal of Medical Genetics
|
August 4, 2025
Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with <i>NF1</i> point variants
Laurence Pacot, Marinus Blok, Dominique Vidaud, et al.
Cancer Discovery
|
April 10, 2022
PD-1 Blockade in Solid Tumors with Defects in Polymerase Epsilon
Benoit Rousseau, Ivan Bieche, Eric Pasmant, et al.
Annales D'Endocrinologie
|
March 21, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions
Laurence Faivre, Camille Level, Régis Coutant, et al.
Annales D'Endocrinologie
|
May 8, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions
Laurence Faivre, Camille Level, Régis Coutant, et al.
Page
of 13