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M Chery

Showing results (11-20 of 26) with videos related to

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Clinical Genetics|December 1, 1985
Mosaic tetrasomy 12pS Gilgenkrantz, P Droulle, M Schweitzer, et al.
British Journal of Haematology|December 31, 1997
De novo methylation of tumour suppressor genes CDKN2A and CDKN2B is a rare finding in B-cell chronic lymphocytic leukaemiaV Martel, A Guerci, J C Humbert, et al.
Human Genetics|May 1, 1994
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpointM Chery, V Biancalana, C Philippe, et al.
Clinical Genetics|September 1, 1995
Monosomy 21q: two cases of del(21q) and review of the literatureJ L Huret, C Léonard, M Chery, et al.
Prenatal Diagnosis|June 1, 1993
Prenatal exclusion of X-linked hydrocephalus-stenosis of the aqueduct of Sylvius sequence using closely linked DNA markersF Serville, P Benit, P Saugier, et al.
Genomics|March 15, 1996
Physical mapping of 49 microsatellite markers on chromosome 19 and correlation with the genetic linkage mapI Reguigne-Arnould, S Faure, M Chery, et al.
Genomics|September 1, 1992
Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS proteinP J Blackshear, J S Tuttle, R J Oakey, et al.
Oncogene|July 1, 1990
Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomasS Gilgenkrantz, M Chery, M Teboul, et al.
Human Genetics|October 1, 1990
Distal trisomy 14q. I. Clinical and cytogenetical studiesS Gilgenkrantz, J Vigneron, M O Peter, et al.
Human Genetics|November 1, 1990
A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1N Abbas, G Novelli, N C Stella, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Clinical Genetics|December 1, 1985
Mosaic tetrasomy 12pS Gilgenkrantz, P Droulle, M Schweitzer, et al.
British Journal of Haematology|December 31, 1997
De novo methylation of tumour suppressor genes CDKN2A and CDKN2B is a rare finding in B-cell chronic lymphocytic leukaemiaV Martel, A Guerci, J C Humbert, et al.
Human Genetics|May 1, 1994
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpointM Chery, V Biancalana, C Philippe, et al.
Clinical Genetics|September 1, 1995
Monosomy 21q: two cases of del(21q) and review of the literatureJ L Huret, C Léonard, M Chery, et al.
Prenatal Diagnosis|June 1, 1993
Prenatal exclusion of X-linked hydrocephalus-stenosis of the aqueduct of Sylvius sequence using closely linked DNA markersF Serville, P Benit, P Saugier, et al.
Genomics|March 15, 1996
Physical mapping of 49 microsatellite markers on chromosome 19 and correlation with the genetic linkage mapI Reguigne-Arnould, S Faure, M Chery, et al.
Genomics|September 1, 1992
Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS proteinP J Blackshear, J S Tuttle, R J Oakey, et al.
Oncogene|July 1, 1990
Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomasS Gilgenkrantz, M Chery, M Teboul, et al.
Human Genetics|October 1, 1990
Distal trisomy 14q. I. Clinical and cytogenetical studiesS Gilgenkrantz, J Vigneron, M O Peter, et al.
Human Genetics|November 1, 1990
A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1N Abbas, G Novelli, N C Stella, et al.
Pageof 3