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Pathologie-Biologie
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February 1, 1977
[Refractory sideroblastic anemia, three cases with the same extra marker chromosome (47, Mar +) (author's transl)]
J F Dor, J F Mattei, M G Mattei, et al.
Lancet (London, England)
|
April 13, 1985
Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome
I Oberlé, J L Mandel, J Boué, et al.
European Journal of Pediatrics
|
February 1, 1984
Bilateral retinoblastoma with de novo constitutional balanced translocation t(2;9)(q11;p11)
P Balestrazzi, M G Mattei, M A Baeteman, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
April 1, 1977
Subacute myelocytic leukemia associated with the philadelphia chromosome and supplementary translocation : 9-12
J F Dor, J F Mattei, M G Mattei, et al.
Nature
|
December 15, 1983
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male
G Camerino, M G Mattei, J F Mattei, et al.
Human Genetics
|
January 1, 1980
Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p
J F Mattei, M G Mattei, J P Ardissone, et al.
Genetical Research
|
June 1, 1989
Chromosomal localization of the mouse gene coding for vimentin
M G Mattei, A Lilienbaum, L Z Lin, et al.
Archives Francaises De Pediatrie
|
February 1, 1975
[Trisomy 8 in mosaicism]
F Giraud, J F Mattei, M Blanc-Pardigon, et al.
Neurosurgical Review
|
July 1, 2011
Critical remarks on the proposed "extended retrosigmoid approach"
Tobias Alecio Mattei, Ricardo Ramina
Cytogenetics and Cell Genetics
|
January 1, 1994
Chromosomal localization of two genes encoding human ras exchange factors: SOS1 maps to the 2p22-->p16 region and SOS2 to the 14q21-->q22 region of the human genome
P Chardin, M G Mattei
Page
of 429
Search research articles
Search
Showing results (241-250 of 4,284) with videos related to
Sort By:
Page
of 429
Pathologie-Biologie
|
February 1, 1977
[Refractory sideroblastic anemia, three cases with the same extra marker chromosome (47, Mar +) (author's transl)]
J F Dor, J F Mattei, M G Mattei, et al.
Lancet (London, England)
|
April 13, 1985
Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome
I Oberlé, J L Mandel, J Boué, et al.
European Journal of Pediatrics
|
February 1, 1984
Bilateral retinoblastoma with de novo constitutional balanced translocation t(2;9)(q11;p11)
P Balestrazzi, M G Mattei, M A Baeteman, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
April 1, 1977
Subacute myelocytic leukemia associated with the philadelphia chromosome and supplementary translocation : 9-12
J F Dor, J F Mattei, M G Mattei, et al.
Nature
|
December 15, 1983
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male
G Camerino, M G Mattei, J F Mattei, et al.
Human Genetics
|
January 1, 1980
Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p
J F Mattei, M G Mattei, J P Ardissone, et al.
Genetical Research
|
June 1, 1989
Chromosomal localization of the mouse gene coding for vimentin
M G Mattei, A Lilienbaum, L Z Lin, et al.
Archives Francaises De Pediatrie
|
February 1, 1975
[Trisomy 8 in mosaicism]
F Giraud, J F Mattei, M Blanc-Pardigon, et al.
Neurosurgical Review
|
July 1, 2011
Critical remarks on the proposed "extended retrosigmoid approach"
Tobias Alecio Mattei, Ricardo Ramina
Cytogenetics and Cell Genetics
|
January 1, 1994
Chromosomal localization of two genes encoding human ras exchange factors: SOS1 maps to the 2p22-->p16 region and SOS2 to the 14q21-->q22 region of the human genome
P Chardin, M G Mattei
Page
of 429