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Showing results (71-80 of 76) with videos related to

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BMJ (Clinical Research Ed.)|May 25, 2004
Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control studyPeadar N Kirke, James L Mills, Anne M Molloy, et al.
ACS Biomaterials Science & Engineering|February 24, 2025
Designing Positionally Stable Smooth Breast ImplantsTim Y Li, Sophia Salingaros, Hector F Salazar, et al.
American Journal of Medical Genetics. Part A|March 26, 2018
Clinical, biochemical, and genetic features of four patients with short-chain enoyl-CoA hydratase (ECHS1) deficiencyPatricia E Fitzsimons, Charlotte L Alston, Penelope E Bonnen, et al.
Heredity|July 30, 2009
The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutationsJ M Flanagan, G McMahon, S H Brendan Chia, et al.
Journal of Inherited Metabolic Disease|October 26, 2016
Guidelines for the diagnosis and management of cystathionine beta-synthase deficiencyAndrew A M Morris, Viktor Kožich, Saikat Santra, et al.
Human Mutation|March 26, 2003
Genetic diversity within the R408W phenylketonuria mutation lineages in EuropeOrna Tighe, Donncha Dunican, Charles O'Neill, et al.
Pageof 8

Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
BMJ (Clinical Research Ed.)|May 25, 2004
Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control studyPeadar N Kirke, James L Mills, Anne M Molloy, et al.
ACS Biomaterials Science & Engineering|February 24, 2025
Designing Positionally Stable Smooth Breast ImplantsTim Y Li, Sophia Salingaros, Hector F Salazar, et al.
American Journal of Medical Genetics. Part A|March 26, 2018
Clinical, biochemical, and genetic features of four patients with short-chain enoyl-CoA hydratase (ECHS1) deficiencyPatricia E Fitzsimons, Charlotte L Alston, Penelope E Bonnen, et al.
Heredity|July 30, 2009
The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutationsJ M Flanagan, G McMahon, S H Brendan Chia, et al.
Journal of Inherited Metabolic Disease|October 26, 2016
Guidelines for the diagnosis and management of cystathionine beta-synthase deficiencyAndrew A M Morris, Viktor Kožich, Saikat Santra, et al.
Human Mutation|March 26, 2003
Genetic diversity within the R408W phenylketonuria mutation lineages in EuropeOrna Tighe, Donncha Dunican, Charles O'Neill, et al.
Pageof 8