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Christophe Philippe

Showing results (1-10 of 150) with videos related to

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European Journal of Human Genetics : EJHG|July 12, 2002
Rapid detection of common autosomal aneuploidies by quantitative fluorescent PCR on uncultured amniocytesHaissam Rahil, Jérome Solassol, Christophe Philippe, et al.
Journal of Pediatric Hematology/Oncology|September 9, 2011
Dysmegakaryopoiesis, a clue for an early diagnosis of familial platelet disorder with propensity to acute myeloid leukemia in case of unexplained inherited thrombocytopenia associated with normal-sized plateletsVéronique Latger-Cannard, Christophe Philippe, Philippe Jonveaux, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|October 8, 2003
MECP2 mutations or polymorphisms in mentally retarded boys: diagnostic implicationsViolaine Bourdon, Christophe Philippe, Dominique Martin, et al.
Human Reproduction (Oxford, England)|March 5, 2003
Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and difficultiesCéline Moutou, Catherine Rongieres, Karima Bettahar-Lebugle, et al.
Soins. Pediatrie, Puericulture|January 14, 2014
[Does the use of psychoactive drugs in adolescence create specific problems?]Raphaël Jeannin, Aymeric Reyre, Christophe Philippe, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Characterization of mosaic supernumerary ring chromosomes by array-CGH: segmental aneusomy for proximal 4q in a child with tall stature and obesityCéline Bonnet, Christian Zix, Marie-José Grégoire, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2000
Polymorphism of angiotensin converting enzyme, angiotensinogen, and angiotensin II type 1 receptor genes and end-stage renal failure in IgA nephropathy: IGARAS--a study of 274 MenLuc Frimat, Christophe Philippe, Marie-Noëlle Maghakian, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Five years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study reporting 95% of the activity in FranceValérie Biancalana, Chérif Beldjord, Agnès Taillandier, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2026
Mild and late onset forms of type I 3-methylglutaconic aciduria presenting as isolated cerebellar ataxia without leukodystrophy: case reports and phenotype expansionFlavie Borel, Christel Thauvin, Manuel Schiff, et al.
Journal of Affective Disorders|November 21, 2020
Cause-specific life years lost in individuals with treatment-resistant depression: A Danish nationwide register-based cohort studyKathrine Bang Madsen, Oleguer Plana-Ripoll, Katherine L Musliner, et al.
Pageof 15

Showing results (1-10 of 150) with videos related to

Sort By:
Pageof 15
European Journal of Human Genetics : EJHG|July 12, 2002
Rapid detection of common autosomal aneuploidies by quantitative fluorescent PCR on uncultured amniocytesHaissam Rahil, Jérome Solassol, Christophe Philippe, et al.
Journal of Pediatric Hematology/Oncology|September 9, 2011
Dysmegakaryopoiesis, a clue for an early diagnosis of familial platelet disorder with propensity to acute myeloid leukemia in case of unexplained inherited thrombocytopenia associated with normal-sized plateletsVéronique Latger-Cannard, Christophe Philippe, Philippe Jonveaux, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|October 8, 2003
MECP2 mutations or polymorphisms in mentally retarded boys: diagnostic implicationsViolaine Bourdon, Christophe Philippe, Dominique Martin, et al.
Human Reproduction (Oxford, England)|March 5, 2003
Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and difficultiesCéline Moutou, Catherine Rongieres, Karima Bettahar-Lebugle, et al.
Soins. Pediatrie, Puericulture|January 14, 2014
[Does the use of psychoactive drugs in adolescence create specific problems?]Raphaël Jeannin, Aymeric Reyre, Christophe Philippe, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Characterization of mosaic supernumerary ring chromosomes by array-CGH: segmental aneusomy for proximal 4q in a child with tall stature and obesityCéline Bonnet, Christian Zix, Marie-José Grégoire, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2000
Polymorphism of angiotensin converting enzyme, angiotensinogen, and angiotensin II type 1 receptor genes and end-stage renal failure in IgA nephropathy: IGARAS--a study of 274 MenLuc Frimat, Christophe Philippe, Marie-Noëlle Maghakian, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Five years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study reporting 95% of the activity in FranceValérie Biancalana, Chérif Beldjord, Agnès Taillandier, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2026
Mild and late onset forms of type I 3-methylglutaconic aciduria presenting as isolated cerebellar ataxia without leukodystrophy: case reports and phenotype expansionFlavie Borel, Christel Thauvin, Manuel Schiff, et al.
Journal of Affective Disorders|November 21, 2020
Cause-specific life years lost in individuals with treatment-resistant depression: A Danish nationwide register-based cohort studyKathrine Bang Madsen, Oleguer Plana-Ripoll, Katherine L Musliner, et al.
Pageof 15