M Prieur - JoVE Visualize

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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.

American Journal of Human Genetics|December 1, 1993

Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial casesC Desmaze, M Prieur, F Amblard, et al.

Human Genetics|January 1, 1985

Inversion (14)(q12qter) or (q11.2q32.3): the most frequently acquired rearrangement in lymphocytesA Aurias, J Couturier, A M Dutrillaux, et al.

American Journal of Medical Genetics. Part A|August 8, 2006

Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterizationP Callier, L Faivre, N Marle, et al.

Clinical Genetics|July 3, 1998

Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndromeG Viot-Szoboszlai, J Amiel, F Doz, et al.

Archives Francaises De Pediatrie|February 1, 1985

[Juvenile chronic arthritis. Double-blind study of the efficacy and tolerance of D-penicillamine]A M Prieur, C Piussan, P Manigne, et al.

Human Genetics|July 1, 1995

Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literatureS Demczuk, A Lévy, M Aubry, 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.

Journal of Immunology (Baltimore, Md. : 1950)|June 8, 2001

Molecular basis of a selective C1s deficiency associated with early onset multiple autoimmune diseasesM A Dragon-Durey, P Quartier, V Frémeaux-Bacchi, et al.

Scandinavian Journal of Rheumatology. Supplement|January 1, 1987

A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patientsA M Prieur, C Griscelli, F Lampert, et al.

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Showing results (131-140 of 183) with videos related to

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Pageof 19

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.

American Journal of Human Genetics|December 1, 1993

Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial casesC Desmaze, M Prieur, F Amblard, et al.

Human Genetics|January 1, 1985

Inversion (14)(q12qter) or (q11.2q32.3): the most frequently acquired rearrangement in lymphocytesA Aurias, J Couturier, A M Dutrillaux, et al.

American Journal of Medical Genetics. Part A|August 8, 2006

Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterizationP Callier, L Faivre, N Marle, et al.

Clinical Genetics|July 3, 1998

Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndromeG Viot-Szoboszlai, J Amiel, F Doz, et al.

Archives Francaises De Pediatrie|February 1, 1985

[Juvenile chronic arthritis. Double-blind study of the efficacy and tolerance of D-penicillamine]A M Prieur, C Piussan, P Manigne, et al.

Human Genetics|July 1, 1995

Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literatureS Demczuk, A Lévy, M Aubry, 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.

Journal of Immunology (Baltimore, Md. : 1950)|June 8, 2001

Molecular basis of a selective C1s deficiency associated with early onset multiple autoimmune diseasesM A Dragon-Durey, P Quartier, V Frémeaux-Bacchi, et al.

Scandinavian Journal of Rheumatology. Supplement|January 1, 1987

A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patientsA M Prieur, C Griscelli, F Lampert, et al.

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