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M Vekemans

Showing results (191-200 of 289) with videos related to

Pageof 29
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Annales De Biologie Clinique|April 19, 2003
[Spectral karyotyping (SKY) principle, avantages and limitations]M A Belaud-Rotureau, H Elghezal, C Bernardin, et al.
Prenatal Diagnosis|February 17, 2001
First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiencyP F Ray, N Gigarel, J P Bonnefont, et al.
Cancer|April 13, 2001
Aspects of intracranial and spinal tumors in patients with Down syndrome and report of a rapidly progressing Grade 2 astrocytomaD Satgé, P Monteil, A J Sasco, et al.
Journal of Medical Genetics|January 1, 1996
Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humansE Treacy, C Polychronakos, M Vekemans, et al.
European Journal of Medical Genetics|June 10, 2006
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate regionM Chaabouni, M Le Merrer, O Raoul, et al.
Journal of Mass Spectrometry : JMS|September 22, 2010
A pitfall of using 2-[(2E)-3-(4-tert-butylphenyl)-2-methylprop-2-enylidene]malononitrile as a matrix in MALDI TOF MS: chemical adduction of matrix to analyte amino groupsXianwen Lou, Bas F M de Waal, Joost L J van Dongen, et al.
Teratology|April 25, 2000
Expression of the sonic hedgehog gene in human embryos with neural tube defectsI Kirillova, I Novikova, J Augé, et al.
British Journal of Haematology|July 23, 1998
Genetic analysis of splenic lymphoma with villous lymphocytes: a Groupe Français d'Hématologie Cellulaire (GFHC) studyX Troussard, L Mauvieux, I Radford-Weiss, et al.
Clinical Genetics|August 16, 2003
PMX2B, a new candidate gene for Hirschsprung's diseaseH K Benailly, J M Lapierre, B Laudier, et al.
Human Molecular Genetics|September 25, 1997
Abnormal FGFR 3 expression in cartilage of thanatophoric dysplasia fetusesA L Delezoide, C Lasselin-Benoist, L Legeai-Mallet, et al.
Pageof 29

Showing results (191-200 of 289) with videos related to

Sort By:
Pageof 29
Annales De Biologie Clinique|April 19, 2003
[Spectral karyotyping (SKY) principle, avantages and limitations]M A Belaud-Rotureau, H Elghezal, C Bernardin, et al.
Prenatal Diagnosis|February 17, 2001
First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiencyP F Ray, N Gigarel, J P Bonnefont, et al.
Cancer|April 13, 2001
Aspects of intracranial and spinal tumors in patients with Down syndrome and report of a rapidly progressing Grade 2 astrocytomaD Satgé, P Monteil, A J Sasco, et al.
Journal of Medical Genetics|January 1, 1996
Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humansE Treacy, C Polychronakos, M Vekemans, et al.
European Journal of Medical Genetics|June 10, 2006
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate regionM Chaabouni, M Le Merrer, O Raoul, et al.
Journal of Mass Spectrometry : JMS|September 22, 2010
A pitfall of using 2-[(2E)-3-(4-tert-butylphenyl)-2-methylprop-2-enylidene]malononitrile as a matrix in MALDI TOF MS: chemical adduction of matrix to analyte amino groupsXianwen Lou, Bas F M de Waal, Joost L J van Dongen, et al.
Teratology|April 25, 2000
Expression of the sonic hedgehog gene in human embryos with neural tube defectsI Kirillova, I Novikova, J Augé, et al.
British Journal of Haematology|July 23, 1998
Genetic analysis of splenic lymphoma with villous lymphocytes: a Groupe Français d'Hématologie Cellulaire (GFHC) studyX Troussard, L Mauvieux, I Radford-Weiss, et al.
Clinical Genetics|August 16, 2003
PMX2B, a new candidate gene for Hirschsprung's diseaseH K Benailly, J M Lapierre, B Laudier, et al.
Human Molecular Genetics|September 25, 1997
Abnormal FGFR 3 expression in cartilage of thanatophoric dysplasia fetusesA L Delezoide, C Lasselin-Benoist, L Legeai-Mallet, et al.
Pageof 29