Search research articles
Contact Us
Filters
Showing results (81-90 of 157) with videos related to
Page
of 16
Sort By:
Genetic Counseling (Geneva, Switzerland)
|
February 19, 2010
Werdnig-Hoffmann disease: report of the first case clinically identified and genetically confirmed in central Africa (Kinshasa-Congo)
A Lumaka, D Bone, R Lukoo, et al.
Journal of Endovascular Therapy : an Official Journal of the International Society of Endovascular Specialists
|
June 8, 2023
Relining of a Bridging Covered Stent to Treat a Rare Cause of Type IIIc Endoleak Following Fenestrated Endovascular Aneurysm Repair
Emiel W M Huistra, Ignace F J Tielliu, G Matthijs Kater, et al.
Heart (British Cardiac Society)
|
June 8, 2010
Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin
A La Gerche, C Robberecht, C Kuiperi, et al.
Journal of Medical Genetics
|
June 1, 1996
Unusual molecular findings in autosomal recessive spinal muscular atrophy
G Matthijs, E Schollen, E Legius, et al.
Human Mutation
|
July 20, 2001
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome
J M Hertz, I Juncker, U Persson, et al.
Prenatal Diagnosis
|
January 26, 2002
Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)
Ingrid Witters, K Devriendt, E Legius, et al.
JIMD Reports
|
February 23, 2013
COG5-CDG with a Mild Neurohepatic Presentation
C W Fung, G Matthijs, L Sturiale, et al.
Familial Cancer
|
June 1, 2006
Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients
M Spaepen, B Vankeirsbilck, S Van Opstal, et al.
Nature Genetics
|
May 1, 1997
Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)
G Matthijs, E Schollen, E Pardon, et al.
Heart (British Cardiac Society)
|
August 9, 2005
The CAREGENE study: ACE gene I/D polymorphism and effect of physical training on aerobic power in coronary artery disease
J Defoor, L Vanhees, K Martens, et al.
Page
of 16
Search research articles
Search
Showing results (81-90 of 157) with videos related to
Sort By:
Page
of 16
Genetic Counseling (Geneva, Switzerland)
|
February 19, 2010
Werdnig-Hoffmann disease: report of the first case clinically identified and genetically confirmed in central Africa (Kinshasa-Congo)
A Lumaka, D Bone, R Lukoo, et al.
Journal of Endovascular Therapy : an Official Journal of the International Society of Endovascular Specialists
|
June 8, 2023
Relining of a Bridging Covered Stent to Treat a Rare Cause of Type IIIc Endoleak Following Fenestrated Endovascular Aneurysm Repair
Emiel W M Huistra, Ignace F J Tielliu, G Matthijs Kater, et al.
Heart (British Cardiac Society)
|
June 8, 2010
Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin
A La Gerche, C Robberecht, C Kuiperi, et al.
Journal of Medical Genetics
|
June 1, 1996
Unusual molecular findings in autosomal recessive spinal muscular atrophy
G Matthijs, E Schollen, E Legius, et al.
Human Mutation
|
July 20, 2001
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome
J M Hertz, I Juncker, U Persson, et al.
Prenatal Diagnosis
|
January 26, 2002
Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)
Ingrid Witters, K Devriendt, E Legius, et al.
JIMD Reports
|
February 23, 2013
COG5-CDG with a Mild Neurohepatic Presentation
C W Fung, G Matthijs, L Sturiale, et al.
Familial Cancer
|
June 1, 2006
Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients
M Spaepen, B Vankeirsbilck, S Van Opstal, et al.
Nature Genetics
|
May 1, 1997
Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)
G Matthijs, E Schollen, E Pardon, et al.
Heart (British Cardiac Society)
|
August 9, 2005
The CAREGENE study: ACE gene I/D polymorphism and effect of physical training on aerobic power in coronary artery disease
J Defoor, L Vanhees, K Martens, et al.
Page
of 16