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Biochemical and Biophysical Research Communications
|
January 13, 1998
Another link between phospholipid transmembrane migration and ABC transporter gene family, inferred from a rare inherited disorder of phosphatidylserine externalization
F Toti, V Schindler, J F Riou, et al.
Human Genetics
|
January 1, 1986
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome
I Oberlé, G Camerino, C Kloepfer, et al.
Clinical Chemistry
|
August 14, 1998
Teaching the microscopic examination of urine sediment to second year medical students using the Urinalysis-Tutor computer program
C Phillips, P J Henderson, L Mandel, et al.
Genomics
|
January 1, 1989
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker
R Fujita, Y Agid, P Trouillas, et al.
Lancet (London, England)
|
March 23, 1985
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs
E Bakker, M H Hofker, N Goor, et al.
The Journal of Surgical Research
|
April 20, 2023
Feasibility of Postoperative Day One or Day Two Discharge After Robotic Cardiac Surgery
Colin C Yost, Jake L Rosen, Jenna L Mandel, et al.
Neurogenetics
|
March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
C Ben Hamida, L Cavalier, S Belal, et al.
Human Molecular Genetics
|
January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region
L J Hu, J Laporte, W Kress, et al.
Genomics
|
January 1, 1991
Genetic mapping of new RFLPs at Xq27-q28
G K Suthers, I Oberlé, J Nancarrow, et al.
Human Mutation
|
May 2, 2000
MTM1 mutations in X-linked myotubular myopathy
J Laporte, V Biancalana, S M Tanner, et al.
Page
of 46
Search research articles
Search
Showing results (421-430 of 451) with videos related to
Sort By:
Page
of 46
Biochemical and Biophysical Research Communications
|
January 13, 1998
Another link between phospholipid transmembrane migration and ABC transporter gene family, inferred from a rare inherited disorder of phosphatidylserine externalization
F Toti, V Schindler, J F Riou, et al.
Human Genetics
|
January 1, 1986
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome
I Oberlé, G Camerino, C Kloepfer, et al.
Clinical Chemistry
|
August 14, 1998
Teaching the microscopic examination of urine sediment to second year medical students using the Urinalysis-Tutor computer program
C Phillips, P J Henderson, L Mandel, et al.
Genomics
|
January 1, 1989
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker
R Fujita, Y Agid, P Trouillas, et al.
Lancet (London, England)
|
March 23, 1985
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs
E Bakker, M H Hofker, N Goor, et al.
The Journal of Surgical Research
|
April 20, 2023
Feasibility of Postoperative Day One or Day Two Discharge After Robotic Cardiac Surgery
Colin C Yost, Jake L Rosen, Jenna L Mandel, et al.
Neurogenetics
|
March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
C Ben Hamida, L Cavalier, S Belal, et al.
Human Molecular Genetics
|
January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region
L J Hu, J Laporte, W Kress, et al.
Genomics
|
January 1, 1991
Genetic mapping of new RFLPs at Xq27-q28
G K Suthers, I Oberlé, J Nancarrow, et al.
Human Mutation
|
May 2, 2000
MTM1 mutations in X-linked myotubular myopathy
J Laporte, V Biancalana, S M Tanner, et al.
Page
of 46