Search research articles
Contact Us
Filters
Showing results (1-10 of 104) with videos related to
Page
of 11
Sort By:
Current Opinion in Genetics & Development
|
June 1, 1995
Finding genes involved in human developmental disorders
M Muenke
Human Mutation
|
August 3, 2000
Mutations in holoprosencephaly
D Wallis, M Muenke
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 22, 1999
The molecular genetics of holoprosencephaly: a model of brain development for the next century
E Roessler, M Muenke
American Journal of Medical Genetics
|
December 1, 1991
High prenatal lead levels and congenital anomalies
M Muenke, F Levine
Molecular Genetics and Metabolism
|
October 21, 1999
Craniosynostosis syndromes: from genes to premature fusion of skull bones
U Hehr, M Muenke
Birth Defects Original Article Series
|
January 1, 1996
The search for genes that cause holoprosencephaly: possible approaches
F Gurrieri, M Muenke
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
October 13, 2001
Midline and laterality defects: left and right meet in the middle
E Roessler, M Muenke
Pediatrics
|
March 1, 1991
VACTERL association with high prenatal lead exposure: similarities to animal models of lead teratogenicity
F Levine, M Muenke
Trends in Genetics : TIG
|
August 1, 1995
Fibroblast-growth-factor receptor mutations in human skeletal disorders
M Muenke, U Schell
Journal of Inherited Metabolic Disease
|
September 5, 1998
Holoprosencephaly: a paradigm for the complex genetics of brain development
E Roessler, M Muenke
Page
of 11
Search research articles
Search
Showing results (1-10 of 104) with videos related to
Sort By:
Page
of 11
Current Opinion in Genetics & Development
|
June 1, 1995
Finding genes involved in human developmental disorders
M Muenke
Human Mutation
|
August 3, 2000
Mutations in holoprosencephaly
D Wallis, M Muenke
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 22, 1999
The molecular genetics of holoprosencephaly: a model of brain development for the next century
E Roessler, M Muenke
American Journal of Medical Genetics
|
December 1, 1991
High prenatal lead levels and congenital anomalies
M Muenke, F Levine
Molecular Genetics and Metabolism
|
October 21, 1999
Craniosynostosis syndromes: from genes to premature fusion of skull bones
U Hehr, M Muenke
Birth Defects Original Article Series
|
January 1, 1996
The search for genes that cause holoprosencephaly: possible approaches
F Gurrieri, M Muenke
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
October 13, 2001
Midline and laterality defects: left and right meet in the middle
E Roessler, M Muenke
Pediatrics
|
March 1, 1991
VACTERL association with high prenatal lead exposure: similarities to animal models of lead teratogenicity
F Levine, M Muenke
Trends in Genetics : TIG
|
August 1, 1995
Fibroblast-growth-factor receptor mutations in human skeletal disorders
M Muenke, U Schell
Journal of Inherited Metabolic Disease
|
September 5, 1998
Holoprosencephaly: a paradigm for the complex genetics of brain development
E Roessler, M Muenke
Page
of 11