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Clinical Genetics
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November 15, 2005
COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology
V A Coronado, J A Bonneville, H Nazer, et al.
Genomics
|
March 15, 1997
Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q
R F Wintle, T G Nygaard, J A Herbrick, et al.
Genomics
|
January 1, 1990
Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency
M H Hofker, S Smith, Y Nakamura, et al.
Irish Medical Journal
|
September 20, 2019
The Prevalence of Pseudomonas Aeruginosa Infection Over a Ten-Year Period in Children with Cystic Fibrosis
K Al Shidhani, R O’Reilly, S Javadpour, et al.
Genomics
|
July 15, 1997
Physical and transcription map in the region 14q24.3: identification of six novel transcripts
A F Roux, J M Rommens, L Read, et al.
Nature Genetics
|
December 1, 1993
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
P C Bull, G R Thomas, J M Rommens, et al.
The Journal of Clinical Investigation
|
December 1, 1990
A null deficiency allele of alpha 1-antitrypsin, QOludwigshafen, with altered tertiary structure
G C Frazier, M A Siewertsen, M H Hofker, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
June 11, 2020
The role of rhinovirus infections in young children with cystic fibrosis
D W O Loughlin, S Coughlan, C F De Gascun, et al.
American Journal of Human Genetics
|
January 1, 1994
Haplotype studies in Wilson disease
G R Thomas, P C Bull, E A Roberts, et al.
Cytogenetics and Cell Genetics
|
January 1, 1994
Regional localization of loci on chromosome 14 using somatic cell hybrids
G D Billingsley, D W Cox, A M Duncan, et al.
Page
of 23
Search research articles
Search
Showing results (171-180 of 223) with videos related to
Sort By:
Page
of 23
Clinical Genetics
|
November 15, 2005
COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology
V A Coronado, J A Bonneville, H Nazer, et al.
Genomics
|
March 15, 1997
Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q
R F Wintle, T G Nygaard, J A Herbrick, et al.
Genomics
|
January 1, 1990
Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency
M H Hofker, S Smith, Y Nakamura, et al.
Irish Medical Journal
|
September 20, 2019
The Prevalence of Pseudomonas Aeruginosa Infection Over a Ten-Year Period in Children with Cystic Fibrosis
K Al Shidhani, R O’Reilly, S Javadpour, et al.
Genomics
|
July 15, 1997
Physical and transcription map in the region 14q24.3: identification of six novel transcripts
A F Roux, J M Rommens, L Read, et al.
Nature Genetics
|
December 1, 1993
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
P C Bull, G R Thomas, J M Rommens, et al.
The Journal of Clinical Investigation
|
December 1, 1990
A null deficiency allele of alpha 1-antitrypsin, QOludwigshafen, with altered tertiary structure
G C Frazier, M A Siewertsen, M H Hofker, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
June 11, 2020
The role of rhinovirus infections in young children with cystic fibrosis
D W O Loughlin, S Coughlan, C F De Gascun, et al.
American Journal of Human Genetics
|
January 1, 1994
Haplotype studies in Wilson disease
G R Thomas, P C Bull, E A Roberts, et al.
Cytogenetics and Cell Genetics
|
January 1, 1994
Regional localization of loci on chromosome 14 using somatic cell hybrids
G D Billingsley, D W Cox, A M Duncan, et al.
Page
of 23