Publications by authors named "Georges Bourrouillou"

8Publications

Distal 10q monosomy: new evidence for a neurobehavioral condition?

Eur J Med Genet 2014 Jan 23;57(1):47-53. Epub 2013 Nov 23.

Service de Génétique Médicale, Hôpital Purpan, Place du Dr Baylac, 31300 Toulouse, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S17697212130025
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http://dx.doi.org/10.1016/j.ejmg.2013.11.002DOI Listing
January 2014

NOTCH, a new signaling pathway implicated in holoprosencephaly.

Hum Mol Genet 2011 Mar 31;20(6):1122-31. Epub 2010 Dec 31.

Institut de Génétique et Développement, CNRS UMR6061, Université de Rennes 1, IFR140 GFAS, Faculté de Médecine, Rennes, France.

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http://dx.doi.org/10.1093/hmg/ddq556DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390777PMC
March 2011

Subtelomeric 6p deletion: clinical, FISH, and array CGH characterization of two cases.

Am J Med Genet A 2005 Jan;132A(2):175-80

Service de Génétique Médicale, Centre Hospitalo-Universitaire, Nantes, France.

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http://dx.doi.org/10.1002/ajmg.a.30409DOI Listing
January 2005

A translocation breakpoint disrupts the ASPM gene in a patient with primary microcephaly.

Eur J Hum Genet 2004 May;12(5):419-21

Service de Génétique Médicale, Hôpital Erasme, Université Libre de Bruxelles, 808 Route de Lennik, 1070 Bruxelles, Belgium.

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http://dx.doi.org/10.1038/sj.ejhg.5201169DOI Listing
May 2004

Maternal serum urea resistant alkaline phosphatase in Down syndrome pregnancy.

Early Hum Dev 2002 Apr;67(1-2):55-9

Laboratoire d'Enzymologie, Service Universitaire d'Hématologie, CHU Rangueil, 31403 Toulouse Cedex 4, France.

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http://dx.doi.org/10.1016/s0378-3782(01)00251-1DOI Listing
April 2002