Search research articles
Contact Us
Filters
Showing results (1-10 of 9) with videos related to
Page
of 1
Sort By:
Human Genetics
|
January 1, 1994
Ordering markers in the region of the ataxia-telangiectasia gene (11q22-q23) by fluorescence in situ hybridization (FISH) to interphase nuclei
D Cherif, H Der-Sarkissian, R Berger
Annales De Genetique
|
January 1, 1986
[Decrease of various enzyme activities in the amniotic fluid of the fetuses with chromosomal anomalies]
F Muller, M Rebiffé, H Der Sarkissian, et al.
Genes, Chromosomes & Cancer
|
February 1, 1993
Chromosome painting in acute monocytic leukemia
D Cherif, S Romana, H Der-Sarkissian, et al.
Cancer Genetics and Cytogenetics
|
September 1, 1982
Sister chromatid exchanges in patients with retinoblastoma
H Der-Sarkissian, Bonaïti-Pellié, M L Briard-Guillemot, et al.
Genes, Chromosomes & Cancer
|
March 1, 1992
The 11q23 breakpoint in acute leukemia with t(11;19)(q23;p13) is distal to those of t(4;11), t(6;11) and t(9;11)
D Cherif, H Der-Sarkissian, J Derré, et al.
La Nouvelle Presse Medicale
|
November 7, 1981
[Antenatal diagnosis of structural chromosome anomalies. 226 cases (author's transl)]
J Boué, F Barichard, C Deluchat, et al.
Leukemia
|
September 20, 2000
Interstitial telomere repeats in translocations of hematopoietic disorders
M Busson Le Coniat, F Brizard, N V Smadja, et al.
Human Molecular Genetics
|
November 18, 1998
NF2 gene in neurofibromatosis type 2 patients
J Zucman-Rossi, P Legoix, H Der Sarkissian, et al.
European Journal of Human Genetics : EJHG
|
March 1, 1997
Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation
T Bienvenu, H Der-Sarkissian, P Billuart, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Human Genetics
|
January 1, 1994
Ordering markers in the region of the ataxia-telangiectasia gene (11q22-q23) by fluorescence in situ hybridization (FISH) to interphase nuclei
D Cherif, H Der-Sarkissian, R Berger
Annales De Genetique
|
January 1, 1986
[Decrease of various enzyme activities in the amniotic fluid of the fetuses with chromosomal anomalies]
F Muller, M Rebiffé, H Der Sarkissian, et al.
Genes, Chromosomes & Cancer
|
February 1, 1993
Chromosome painting in acute monocytic leukemia
D Cherif, S Romana, H Der-Sarkissian, et al.
Cancer Genetics and Cytogenetics
|
September 1, 1982
Sister chromatid exchanges in patients with retinoblastoma
H Der-Sarkissian, Bonaïti-Pellié, M L Briard-Guillemot, et al.
Genes, Chromosomes & Cancer
|
March 1, 1992
The 11q23 breakpoint in acute leukemia with t(11;19)(q23;p13) is distal to those of t(4;11), t(6;11) and t(9;11)
D Cherif, H Der-Sarkissian, J Derré, et al.
La Nouvelle Presse Medicale
|
November 7, 1981
[Antenatal diagnosis of structural chromosome anomalies. 226 cases (author's transl)]
J Boué, F Barichard, C Deluchat, et al.
Leukemia
|
September 20, 2000
Interstitial telomere repeats in translocations of hematopoietic disorders
M Busson Le Coniat, F Brizard, N V Smadja, et al.
Human Molecular Genetics
|
November 18, 1998
NF2 gene in neurofibromatosis type 2 patients
J Zucman-Rossi, P Legoix, H Der Sarkissian, et al.
European Journal of Human Genetics : EJHG
|
March 1, 1997
Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation
T Bienvenu, H Der-Sarkissian, P Billuart, et al.
Page
of 1