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Genes, Chromosomes & Cancer|February 15, 2001
Molecular cytogenetic and clinical findings in ETV6/ABL1-positive leukemiaH Van Limbergen, H B Beverloo, E van Drunen, et al.Blood|July 15, 1996
Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromesS D Raynaud, M Baens, J Grosgeorge, 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 originA La Gerche, C Robberecht, C Kuiperi, et al.Journal of Medical Genetics|June 1, 1996
Unusual molecular findings in autosomal recessive spinal muscular atrophyG 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 syndromeJ 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.Clinical Genetics|October 30, 2009
Novel PORCN mutations in focal dermal hypoplasiaG Froyen, K Govaerts, H Van Esch, et al.JIMD Reports|February 23, 2013
COG5-CDG with a Mild Neurohepatic PresentationC 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) patientsM 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.Pageof 28