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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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J M Lapierre

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Clinical Genetics|August 16, 2003

PMX2B, a new candidate gene for Hirschsprung's diseaseH K Benailly, J M Lapierre, B Laudier, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 13, 2005

[Microarray CGH: principle and use for constitutional disorders]D Sanlaville, J M Lapierre, A Coquin, et al.

American Journal of Medical Genetics|November 29, 2002

Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literatureS Brisset, G Joly, C Ozilou, 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.

Annales De Genetique|December 2, 1998

Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalitiesJ M Lapierre, V Cacheux, N Collot, et al.

The Journal of Biological Chemistry|April 20, 2000

Identification of the binding site for a novel class of CCR2b chemokine receptor antagonists: binding to a common chemokine receptor motif within the helical bundleT Mirzadegan, F Diehl, B Ebi, et al.

Clinical Genetics|October 12, 2001

Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeG Joly, J M Lapierre, C Ozilou, et al.

Clinical Genetics|April 10, 2002

A CGH study of 27 patients with CHARGE associationD Sanlaville, S P Romana, J M Lapierre, et al.

Journal of Medical Genetics|August 6, 2002

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotypeL Faivre, V Cormier-Daire, J M Lapierre, et al.

Annales De Biologie Clinique|March 30, 2004

[A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances]J-M Lapierre, D Sanlaville, J Kang, et al.

Pageof 2

Search research articles

Showing results (11-20 of 20) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 20 results.

Clinical Genetics|August 16, 2003

PMX2B, a new candidate gene for Hirschsprung's diseaseH K Benailly, J M Lapierre, B Laudier, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 13, 2005

[Microarray CGH: principle and use for constitutional disorders]D Sanlaville, J M Lapierre, A Coquin, et al.

American Journal of Medical Genetics|November 29, 2002

Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literatureS Brisset, G Joly, C Ozilou, 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.

Annales De Genetique|December 2, 1998

The Journal of Biological Chemistry|April 20, 2000

Clinical Genetics|October 12, 2001

Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeG Joly, J M Lapierre, C Ozilou, et al.

Clinical Genetics|April 10, 2002

A CGH study of 27 patients with CHARGE associationD Sanlaville, S P Romana, J M Lapierre, et al.

Journal of Medical Genetics|August 6, 2002

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotypeL Faivre, V Cormier-Daire, J M Lapierre, et al.

Annales De Biologie Clinique|March 30, 2004

[A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances]J-M Lapierre, D Sanlaville, J Kang, et al.

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