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Biochemical Genetics
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February 1, 1980
Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants
J Camakaris, D M Danks, L Ackland, et al.
The American Journal of Physiology
|
April 1, 1989
Effect of chelators on copper metabolism and copper pools in mouse hepatocytes
H J McArdle, S M Gross, I Creaser, et al.
Biochemical Genetics
|
October 1, 1980
Genetics of mammalian phenylalanine hydroxylase system. IV. Evidence of phenylalanine hydroxylase in a cultured human hepatoma cell line
K H Choo, R G Cotton, I G Jennings, et al.
Human Mutation
|
January 1, 1997
DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient
K Takayama, D M Danks, E P Salazar, et al.
American Journal of Medical Genetics
|
February 1, 1990
Geleophysic dysplasia
J E Wraith, A Bankier, C W Chow, et al.
Prenatal Diagnosis
|
May 1, 1995
New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined population
J L Halliday, L F Watson, J Lumley, et al.
European Journal of Pediatrics
|
October 1, 1988
Maternal phenylketonuria: successful outcome in four pregnancies treated prior to conception
B C Lynch, D B Pitt, T G Maddison, et al.
American Journal of Diseases of Children (1960)
|
November 1, 1974
Extrahepatic biliary atresia: the frequency of potentially operable cases
D M Danks, P E Campbell, A M Clarke, et al.
Acta Neuropathologica
|
January 1, 1985
Congenital absence of pyramids and its significance in genetic diseases
C W Chow, J L Halliday, R M Anderson, et al.
The Journal of Investigative Dermatology
|
March 1, 1996
Hairs from patients with maple syrup urine disease show a structural defect in the fiber cuticle
L N Jones, D J Peet, D M Danks, et al.
Page
of 26
Search research articles
Search
Showing results (201-210 of 255) with videos related to
Sort By:
Page
of 26
Biochemical Genetics
|
February 1, 1980
Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants
J Camakaris, D M Danks, L Ackland, et al.
The American Journal of Physiology
|
April 1, 1989
Effect of chelators on copper metabolism and copper pools in mouse hepatocytes
H J McArdle, S M Gross, I Creaser, et al.
Biochemical Genetics
|
October 1, 1980
Genetics of mammalian phenylalanine hydroxylase system. IV. Evidence of phenylalanine hydroxylase in a cultured human hepatoma cell line
K H Choo, R G Cotton, I G Jennings, et al.
Human Mutation
|
January 1, 1997
DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient
K Takayama, D M Danks, E P Salazar, et al.
American Journal of Medical Genetics
|
February 1, 1990
Geleophysic dysplasia
J E Wraith, A Bankier, C W Chow, et al.
Prenatal Diagnosis
|
May 1, 1995
New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined population
J L Halliday, L F Watson, J Lumley, et al.
European Journal of Pediatrics
|
October 1, 1988
Maternal phenylketonuria: successful outcome in four pregnancies treated prior to conception
B C Lynch, D B Pitt, T G Maddison, et al.
American Journal of Diseases of Children (1960)
|
November 1, 1974
Extrahepatic biliary atresia: the frequency of potentially operable cases
D M Danks, P E Campbell, A M Clarke, et al.
Acta Neuropathologica
|
January 1, 1985
Congenital absence of pyramids and its significance in genetic diseases
C W Chow, J L Halliday, R M Anderson, et al.
The Journal of Investigative Dermatology
|
March 1, 1996
Hairs from patients with maple syrup urine disease show a structural defect in the fiber cuticle
L N Jones, D J Peet, D M Danks, et al.
Page
of 26