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Gastroenterology
|
January 1, 1996
Aberrant expression of a human mucin gene (MUC5AC) in rectosigmoid villous adenoma
M P Buisine, A Janin, V Maunoury, et al.
Human Genetics
|
April 17, 1998
Variable number tandem repeat polymorphism of the mucin genes located in the complex on 11p15.5
L E Vinall, A S Hill, P Pigny, et al.
Clinical Chemistry
|
July 27, 2001
Heterozygous M3Mmalton alpha1-antitrypsin deficiency associated with end-stage liver disease: case report and review
V Canva, S Piotte, J P Aubert, et al.
Annales De Chirurgie
|
March 24, 2005
[Paragangliomas: clinical and secretory profile. Result of 39 cases]
A Lamblin, P Pigny, G Tex, et al.
Clinical Genetics
|
September 6, 2013
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause
F Petit, F Escande, A S Jourdain, et al.
American Journal of Respiratory Cell and Molecular Biology
|
November 4, 2000
Polymorphism of human mucin genes in chest disease: possible significance of MUC2
L E Vinall, J C Fowler, A L Jones, et al.
Genomics
|
December 15, 1996
Human mucin genes assigned to 11p15.5: identification and organization of a cluster of genes
P Pigny, V Guyonnet-Duperat, A S Hill, et al.
Clinical Genetics
|
June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new families
F Petit, A-S Jourdain, J Andrieux, et al.
American Journal of Human Genetics
|
July 31, 1998
Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders
S Giraud, C X Zhang, O Serova-Sinilnikova, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 89) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 89 results.
Gastroenterology
|
January 1, 1996
Aberrant expression of a human mucin gene (MUC5AC) in rectosigmoid villous adenoma
M P Buisine, A Janin, V Maunoury, et al.
Human Genetics
|
April 17, 1998
Variable number tandem repeat polymorphism of the mucin genes located in the complex on 11p15.5
L E Vinall, A S Hill, P Pigny, et al.
Clinical Chemistry
|
July 27, 2001
Heterozygous M3Mmalton alpha1-antitrypsin deficiency associated with end-stage liver disease: case report and review
V Canva, S Piotte, J P Aubert, et al.
Annales De Chirurgie
|
March 24, 2005
[Paragangliomas: clinical and secretory profile. Result of 39 cases]
A Lamblin, P Pigny, G Tex, et al.
Clinical Genetics
|
September 6, 2013
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause
F Petit, F Escande, A S Jourdain, et al.
American Journal of Respiratory Cell and Molecular Biology
|
November 4, 2000
Polymorphism of human mucin genes in chest disease: possible significance of MUC2
L E Vinall, J C Fowler, A L Jones, et al.
Genomics
|
December 15, 1996
Human mucin genes assigned to 11p15.5: identification and organization of a cluster of genes
P Pigny, V Guyonnet-Duperat, A S Hill, et al.
Clinical Genetics
|
June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new families
F Petit, A-S Jourdain, J Andrieux, et al.
American Journal of Human Genetics
|
July 31, 1998
Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders
S Giraud, C X Zhang, O Serova-Sinilnikova, et al.
Page
of 9