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Human Genetics
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December 3, 2003
Gene symbol: IRF6. Disease: Van der Woude syndrome
M Ghassibe, N Revencu, B Bayet, et al.
Gastroenterology
|
December 28, 1999
The A16V signal peptide cleavage site mutation in the cationic trypsinogen gene and chronic pancreatitis
J M Chen, O Raguenes, C Ferec, et al.
Acta Urologica Belgica
|
December 1, 1993
Autosomal dominant polycystic kidney disease in the first year of life. Report of a case with no family history
J P Stalens, E Sokal, C Walon, et al.
Journal of Medical Genetics
|
February 6, 2004
Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene
M Ghassibé, N Revencu, B Bayet, et al.
British Journal of Plastic Surgery
|
May 1, 1988
Congenital ring-constriction syndrome of the limbs; a report of 19 cases
D Rossillon, J J Rombouts, C Verellen-Dumoulin, et al.
Hepatology (Baltimore, Md.)
|
February 1, 1996
Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2
Y Pirson, N Lannoy, D Peters, et al.
Chest
|
March 13, 2001
Frequency of cystic fibrosis transmembrane conductance regulator gene mutations and 5T allele in patients with allergic bronchopulmonary aspergillosis
E Marchand, C Verellen-Dumoulin, M Mairesse, et al.
Acta Gastro-Enterologica Belgica
|
September 1, 1992
[Familial adenomatous polyposis: what is new for the clinician?]
J P Coppens, A Kartheuser, C Verellen-Dumoulin, et al.
Clinical Dysmorphology
|
January 1, 1996
A new familial short stature syndrome: Brussels type
C Mievis, D Claus, P Clapuyt, et al.
Mutation Research
|
March 1, 1993
Increased sister chromatid exchanges and tumor markers in workers exposed to elemental chromium-, cobalt- and nickel-containing dusts
J P Gennart, C Baleux, C Verellen-Dumoulin, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 77) with videos related to
Sort By:
Page
of 8
Human Genetics
|
December 3, 2003
Gene symbol: IRF6. Disease: Van der Woude syndrome
M Ghassibe, N Revencu, B Bayet, et al.
Gastroenterology
|
December 28, 1999
The A16V signal peptide cleavage site mutation in the cationic trypsinogen gene and chronic pancreatitis
J M Chen, O Raguenes, C Ferec, et al.
Acta Urologica Belgica
|
December 1, 1993
Autosomal dominant polycystic kidney disease in the first year of life. Report of a case with no family history
J P Stalens, E Sokal, C Walon, et al.
Journal of Medical Genetics
|
February 6, 2004
Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene
M Ghassibé, N Revencu, B Bayet, et al.
British Journal of Plastic Surgery
|
May 1, 1988
Congenital ring-constriction syndrome of the limbs; a report of 19 cases
D Rossillon, J J Rombouts, C Verellen-Dumoulin, et al.
Hepatology (Baltimore, Md.)
|
February 1, 1996
Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2
Y Pirson, N Lannoy, D Peters, et al.
Chest
|
March 13, 2001
Frequency of cystic fibrosis transmembrane conductance regulator gene mutations and 5T allele in patients with allergic bronchopulmonary aspergillosis
E Marchand, C Verellen-Dumoulin, M Mairesse, et al.
Acta Gastro-Enterologica Belgica
|
September 1, 1992
[Familial adenomatous polyposis: what is new for the clinician?]
J P Coppens, A Kartheuser, C Verellen-Dumoulin, et al.
Clinical Dysmorphology
|
January 1, 1996
A new familial short stature syndrome: Brussels type
C Mievis, D Claus, P Clapuyt, et al.
Mutation Research
|
March 1, 1993
Increased sister chromatid exchanges and tumor markers in workers exposed to elemental chromium-, cobalt- and nickel-containing dusts
J P Gennart, C Baleux, C Verellen-Dumoulin, et al.
Page
of 8