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Pediatric Radiology
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January 1, 1994
Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasia
J Spranger, H Menger, S Mundlos, et al.
Klinische Padiatrie
|
May 1, 1992
[Clinical importance of hepatitis B virus DNA detection in serum of children with chronic hepatitis B]
S Wirth, U Möllers, E Schaefer, et al.
The Journal of Clinical Investigation
|
November 1, 1991
Molecular genetics of intestinal glucose transport
E M Wright, E Turk, B Zabel, et al.
Humangenetik
|
January 1, 1974
Supernumerary small ring chromosome
J J Hoo, C Forster, I Kindermann, et al.
Genomics
|
December 10, 1999
Isolation, characterization, and mapping of a zinc finger gene, ZFP95, containing both a SCAN box and an alternatively spliced KRAB A domain
S D Dreyer, Q Zheng, B Zabel, et al.
Nature
|
March 28, 1991
Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter
E Turk, B Zabel, S Mundlos, et al.
Genetic Counseling (Geneva, Switzerland)
|
December 3, 2015
A NOVEL MUTATION ASSOCIATED WITH NEPHROLITIHASIS IN ELLIS-VAN CREVELD SYNDROME
A Kiraz, M A Akin, A Arslan, et al.
The International Journal of Developmental Biology
|
December 1, 1996
Developmental expression of splicing variants of fibroblast growth factor receptor 3 (FGFR3) in mouse
C Wuechner, A C Nordqvist, A Winterpacht, et al.
American Journal of Medical Genetics. Part A
|
November 20, 2004
A disorder resembling pseudoachondroplasia but without COMP mutation
J W Spranger, B Zabel, J Kennedy, et al.
Hepatology (Baltimore, Md.)
|
March 30, 1999
Mutations in the basic core promotor and the precore region of hepatitis B virus and their selection in children with fulminant and chronic hepatitis B
M Friedt, P Gerner, E Lausch, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 120) with videos related to
Sort By:
Page
of 12
Pediatric Radiology
|
January 1, 1994
Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasia
J Spranger, H Menger, S Mundlos, et al.
Klinische Padiatrie
|
May 1, 1992
[Clinical importance of hepatitis B virus DNA detection in serum of children with chronic hepatitis B]
S Wirth, U Möllers, E Schaefer, et al.
The Journal of Clinical Investigation
|
November 1, 1991
Molecular genetics of intestinal glucose transport
E M Wright, E Turk, B Zabel, et al.
Humangenetik
|
January 1, 1974
Supernumerary small ring chromosome
J J Hoo, C Forster, I Kindermann, et al.
Genomics
|
December 10, 1999
Isolation, characterization, and mapping of a zinc finger gene, ZFP95, containing both a SCAN box and an alternatively spliced KRAB A domain
S D Dreyer, Q Zheng, B Zabel, et al.
Nature
|
March 28, 1991
Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter
E Turk, B Zabel, S Mundlos, et al.
Genetic Counseling (Geneva, Switzerland)
|
December 3, 2015
A NOVEL MUTATION ASSOCIATED WITH NEPHROLITIHASIS IN ELLIS-VAN CREVELD SYNDROME
A Kiraz, M A Akin, A Arslan, et al.
The International Journal of Developmental Biology
|
December 1, 1996
Developmental expression of splicing variants of fibroblast growth factor receptor 3 (FGFR3) in mouse
C Wuechner, A C Nordqvist, A Winterpacht, et al.
American Journal of Medical Genetics. Part A
|
November 20, 2004
A disorder resembling pseudoachondroplasia but without COMP mutation
J W Spranger, B Zabel, J Kennedy, et al.
Hepatology (Baltimore, Md.)
|
March 30, 1999
Mutations in the basic core promotor and the precore region of hepatitis B virus and their selection in children with fulminant and chronic hepatitis B
M Friedt, P Gerner, E Lausch, et al.
Page
of 12