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The Journal of Clinical Investigation
|
August 15, 1996
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency
M E Chamberlin, T Ubagai, S H Mudd, et al.
Journal of Medical Genetics
|
July 1, 1995
Molecular analysis of three patients with interstitial deletions of chromosome band 14q31
B C Byth, M T Costa, I E Teshima, et al.
American Journal of Medical Genetics
|
September 1, 1983
Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations
W G Wilson, M A Shires, K A Willson, et al.
American Journal of Medical Genetics
|
November 1, 1987
Deletion (13)(q14.1q14.3) in two generations: variability of ocular manifestations and definition of the phenotype
W G Wilson, P A Campochiaro, B P Conway, et al.
Prenatal Diagnosis
|
December 18, 2001
Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changes
C A Chisholm, F Vavelidis, M A Lovell, et al.
Radiology
|
June 1, 1990
Spondylometaphyseal dysplasia, corner fracture type: a heritable condition associated with coxa vara
L O Langer, P W Brill, M B Ozonoff, et al.
American Journal of Human Genetics
|
October 1, 1995
Isolated persistent hypermethioninemia
S H Mudd, H L Levy, A Tangerman, et al.
Annals of Neurology
|
July 17, 1998
Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations
Y Furukawa, S J Kish, E M Bebin, et al.
Neurology
|
May 1, 1997
Oral phenylalanine loading in dopa-responsive dystonia: a possible diagnostic test
K Hyland, J S Fryburg, W G Wilson, et al.
Human Molecular Genetics
|
February 1, 1996
Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21
U Schell, J Wienberg, A Köhler, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 70) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 70 results.
The Journal of Clinical Investigation
|
August 15, 1996
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency
M E Chamberlin, T Ubagai, S H Mudd, et al.
Journal of Medical Genetics
|
July 1, 1995
Molecular analysis of three patients with interstitial deletions of chromosome band 14q31
B C Byth, M T Costa, I E Teshima, et al.
American Journal of Medical Genetics
|
September 1, 1983
Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations
W G Wilson, M A Shires, K A Willson, et al.
American Journal of Medical Genetics
|
November 1, 1987
Deletion (13)(q14.1q14.3) in two generations: variability of ocular manifestations and definition of the phenotype
W G Wilson, P A Campochiaro, B P Conway, et al.
Prenatal Diagnosis
|
December 18, 2001
Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changes
C A Chisholm, F Vavelidis, M A Lovell, et al.
Radiology
|
June 1, 1990
Spondylometaphyseal dysplasia, corner fracture type: a heritable condition associated with coxa vara
L O Langer, P W Brill, M B Ozonoff, et al.
American Journal of Human Genetics
|
October 1, 1995
Isolated persistent hypermethioninemia
S H Mudd, H L Levy, A Tangerman, et al.
Annals of Neurology
|
July 17, 1998
Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations
Y Furukawa, S J Kish, E M Bebin, et al.
Neurology
|
May 1, 1997
Oral phenylalanine loading in dopa-responsive dystonia: a possible diagnostic test
K Hyland, J S Fryburg, W G Wilson, et al.
Human Molecular Genetics
|
February 1, 1996
Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21
U Schell, J Wienberg, A Köhler, et al.
Page
of 7