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Anemia|July 11, 2012
Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger SequencingJohan J P Gille, Karijn Floor, Lianne Kerkhoven, et al.Breast Cancer Research and Treatment|June 29, 2010
PALB2 analysis in BRCA2-like familiesM A Adank, S E van Mil, J J P Gille, et al.Prenatal Diagnosis|November 27, 2004
Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma--case reportY Li, W Holzgreve, G C M L Page-Christiaens, et al.Prenatal Diagnosis|December 13, 2006
Non-invasive prenatal detection of achondroplasia in size-fractionated cell-free DNA by MALDI-TOF MS assayYing Li, Godelieve C M L Page-Christiaens, Johan J P Gille, et al.Respiration Physiology|January 1, 1995
Vascular distension in muscles contributes to respiratory control in sheepP Haouzi, A Huszczuk, J P Gille, et al.Bulletin Europeen De Physiopathologie Respiratoire|November 1, 1982
[Experimental chronic paraquat poisoning. Functional and histopathological pulmonary changes]C Saunier, F Schrijen, J P Gille, et al.Respiration; International Review of Thoracic Diseases|January 1, 1988
Cardiorespiratory function and pathological findings in heart-lung block reimplanted after hypothermic preservationC Saunier, J P Gille, J P Villemot, et al.Journal of Community Genetics|September 20, 2018
Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluationKim C A Holtkamp, Lidewij Henneman, Johan J P Gille, et al.European Journal of Medical Research|June 19, 2008
Surfactant protein B deficiency caused by a novel mutation involving multiple exons of the SP-B geneF A B A Schuerman, M Griese, J P Gille, et al.Familial Cancer|September 2, 2004
A homozygous MSH6 mutation in a child with café-au-lait spots, oligodendroglioma and rectal cancerFred H Menko, Gertjan L Kaspers, Gerrit A Meijer, et al.Pageof 11