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M Vekemans

Showing results (221-230 of 289) with videos related to

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Organic & Biomolecular Chemistry|May 18, 2012
Helical self-assembly and co-assembly of fluorinated, preorganized discoticsMichel H C J van Houtem, Faysal Benaskar, Carel F C Fitié, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 28, 2002
[What's new in fetal medicine?]D Mahieu-Caputo, M V Senat, S Romana, et al.
American Journal of Medical Genetics|February 15, 1994
U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8J J Mitchell, M Vekemans, S Luscombe, et al.
Journal of Medical Genetics|December 14, 2004
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndromeG Borck, R Redon, D Sanlaville, et al.
American Journal of Medical Genetics|January 8, 1999
Expression of the RET proto-oncogene in human embryosT Attié-Bitach, M Abitbol, M Gérard, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Leukemia|November 17, 2007
Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocationG Soler, I Radford-Weiss, R Ben-Abdelali, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
Mild phenotype in a 15-year-old boy with Pallister-Killian syndromeD Genevieve, V Cormier-Daire, D Sanlaville, et al.
Journal of Mass Spectrometry : JMS|March 6, 2008
Dehydrogenation of tertiary amines in matrix-assisted laser desorption/ionization time-of-flight mass spectrometryXianwen Lou, A J H Spiering, Bas F M de Waal, et al.
Journal of Medical Genetics|July 7, 2000
Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow upD Sanlaville, M C Aubry, Y Dumez, et al.
Pageof 29

Showing results (221-230 of 289) with videos related to

Sort By:
Pageof 29
Organic & Biomolecular Chemistry|May 18, 2012
Helical self-assembly and co-assembly of fluorinated, preorganized discoticsMichel H C J van Houtem, Faysal Benaskar, Carel F C Fitié, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 28, 2002
[What's new in fetal medicine?]D Mahieu-Caputo, M V Senat, S Romana, et al.
American Journal of Medical Genetics|February 15, 1994
U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8J J Mitchell, M Vekemans, S Luscombe, et al.
Journal of Medical Genetics|December 14, 2004
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndromeG Borck, R Redon, D Sanlaville, et al.
American Journal of Medical Genetics|January 8, 1999
Expression of the RET proto-oncogene in human embryosT Attié-Bitach, M Abitbol, M Gérard, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Leukemia|November 17, 2007
Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocationG Soler, I Radford-Weiss, R Ben-Abdelali, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
Mild phenotype in a 15-year-old boy with Pallister-Killian syndromeD Genevieve, V Cormier-Daire, D Sanlaville, et al.
Journal of Mass Spectrometry : JMS|March 6, 2008
Dehydrogenation of tertiary amines in matrix-assisted laser desorption/ionization time-of-flight mass spectrometryXianwen Lou, A J H Spiering, Bas F M de Waal, et al.
Journal of Medical Genetics|July 7, 2000
Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow upD Sanlaville, M C Aubry, Y Dumez, et al.
Pageof 29