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M Vekemans

Showing results (211-220 of 289) with videos related to

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Journal De La Societe De Biologie|April 28, 2001
[Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy]J Amiel, R Salomon, T Attié-Bitach, et al.
Revue Medicale De Bruxelles|November 1, 1985
[2 years' activity in in vitro fertilization: methods of presenting results]M Camus, B Lejeune, F Puissant, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndromeV Cormier-Daire, V Belin, V Cusin, et al.
Prenatal Diagnosis|January 11, 2008
Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasiaGeneviève Quenum-Miraillet, Valérie Malan, Jelena Martinovic, et al.
Blood|August 1, 1997
A chromosome 14q11/TCR alpha/delta specific yeast artificial chromosome improves the detection rate and characterization of chromosome abnormalities in T-lymphoproliferative disordersK A Rack, F Cornélis, I Radford-Weiss, et al.
Nature Genetics|May 20, 1998
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)V Belin, V Cusin, G Viot, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Kidney International|February 13, 2001
PAX2 mutations in oligomeganephroniaR Salomon, A L Tellier, T Attie-Bitach, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|March 10, 2001
[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities]S P Romana, P Gosset, H Elghezal, et al.
The Journal of Clinical Endocrinology and Metabolism|January 3, 2001
Temporal and spatial association of matrix metalloproteinases with focal endometrial breakdown and bleeding upon progestin-only contraceptionC Galant, M Vekemans, P Lemoine, et al.
Pageof 29

Showing results (211-220 of 289) with videos related to

Sort By:
Pageof 29
Journal De La Societe De Biologie|April 28, 2001
[Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy]J Amiel, R Salomon, T Attié-Bitach, et al.
Revue Medicale De Bruxelles|November 1, 1985
[2 years' activity in in vitro fertilization: methods of presenting results]M Camus, B Lejeune, F Puissant, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndromeV Cormier-Daire, V Belin, V Cusin, et al.
Prenatal Diagnosis|January 11, 2008
Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasiaGeneviève Quenum-Miraillet, Valérie Malan, Jelena Martinovic, et al.
Blood|August 1, 1997
A chromosome 14q11/TCR alpha/delta specific yeast artificial chromosome improves the detection rate and characterization of chromosome abnormalities in T-lymphoproliferative disordersK A Rack, F Cornélis, I Radford-Weiss, et al.
Nature Genetics|May 20, 1998
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)V Belin, V Cusin, G Viot, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Kidney International|February 13, 2001
PAX2 mutations in oligomeganephroniaR Salomon, A L Tellier, T Attie-Bitach, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|March 10, 2001
[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities]S P Romana, P Gosset, H Elghezal, et al.
The Journal of Clinical Endocrinology and Metabolism|January 3, 2001
Temporal and spatial association of matrix metalloproteinases with focal endometrial breakdown and bleeding upon progestin-only contraceptionC Galant, M Vekemans, P Lemoine, et al.
Pageof 29