Search research articles
Contact Us
Filters
Showing results (41-50 of 56) with videos related to
Page
of 6
Sort By:
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation
L Strain, M E Porteous, C M Gosden, et al.
Diabetologia
|
May 10, 2003
Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasians
M Veiga-da-Cunha, J Delplanque, A Gillain, et al.
BMC Genetics
|
January 28, 2003
Lack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germline
B E Hayward, M De Vos, H Judson, et al.
Journal of Medical Genetics
|
September 10, 2003
Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3
S Brickwood, D T Bonthron, L I Al-Gazali, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
June 1, 1996
Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of chromosome 2p23
B E Hayward, J A Fantes, J P Warner, et al.
Science (New York, N.Y.)
|
June 21, 1985
Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization
D Ginsburg, R I Handin, D T Bonthron, et al.
Genomics
|
May 8, 1998
Organization of the human glucokinase regulator gene GCKR
B E Hayward, N Dunlop, S Intody, et al.
American Journal of Human Genetics
|
July 27, 1999
A locus for isolated cleft palate, located on human chromosome 2q32
C M Brewer, J P Leek, A J Green, et al.
Biochemical Society Transactions
|
February 1, 1997
Molecular genetics of the human glucokinase regulator-fructokinase (GCKR-KHK) region of chromosome 2p23
B E Hayward, J P Warner, N Dunlop, et al.
Clinical Endocrinology
|
January 7, 1999
GNAS1 mutational analysis in pseudohypoparathyroidism
S F Ahmed, P H Dixon, D T Bonthron, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 56) with videos related to
Sort By:
Page
of 6
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation
L Strain, M E Porteous, C M Gosden, et al.
Diabetologia
|
May 10, 2003
Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasians
M Veiga-da-Cunha, J Delplanque, A Gillain, et al.
BMC Genetics
|
January 28, 2003
Lack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germline
B E Hayward, M De Vos, H Judson, et al.
Journal of Medical Genetics
|
September 10, 2003
Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3
S Brickwood, D T Bonthron, L I Al-Gazali, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
June 1, 1996
Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of chromosome 2p23
B E Hayward, J A Fantes, J P Warner, et al.
Science (New York, N.Y.)
|
June 21, 1985
Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization
D Ginsburg, R I Handin, D T Bonthron, et al.
Genomics
|
May 8, 1998
Organization of the human glucokinase regulator gene GCKR
B E Hayward, N Dunlop, S Intody, et al.
American Journal of Human Genetics
|
July 27, 1999
A locus for isolated cleft palate, located on human chromosome 2q32
C M Brewer, J P Leek, A J Green, et al.
Biochemical Society Transactions
|
February 1, 1997
Molecular genetics of the human glucokinase regulator-fructokinase (GCKR-KHK) region of chromosome 2p23
B E Hayward, J P Warner, N Dunlop, et al.
Clinical Endocrinology
|
January 7, 1999
GNAS1 mutational analysis in pseudohypoparathyroidism
S F Ahmed, P H Dixon, D T Bonthron, et al.
Page
of 6