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Human Genetics
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January 19, 1979
Origin of the extra chromosome in trisomy 21
J F Mattei, M G Mattei, S Ayme, et al.
Human Genetics
|
January 1, 1981
Partial inversion of the secondary constriction of chromosome 9. Does it exist?
M G Mattei, J F Mattei, M Guichaoua, et al.
Human Genetics
|
January 1, 1981
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approach
M G Mattei, J F Mattei, I Vidal, et al.
Pediatrie
|
July 1, 1971
[Lyell syndrome and its sequelae in an asthmatic child]
E Louchet, L A Gratecos, C Paoli, et al.
Clinical Genetics
|
September 1, 1983
Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletion
J F Mattei, M G Mattei, P Balestrazzi, et al.
Journal De Genetique Humaine
|
March 1, 1982
[Interstitial deletion of chromosome 7 (7q33 to q35)]
M Arnolds, M G Mattei, P Rebuffel, et al.
Human Genetics
|
January 1, 1982
X-autosome translocations: cytogenetic characteristics and their consequences
M G Mattei, J F Mattei, S Ayme, et al.
Human Genetics
|
September 2, 1979
Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation
M G Mattei, J F Mattei, R Bernard, et al.
Human Genetics
|
October 28, 1976
Constitutional chromosomal breakage
F Giraud, S Ayme, J F Mattei, et al.
Humangenetik
|
August 25, 1975
[Partial trisomy 11q and familial translocation 11--22 (author's transl)]
F Giraud, J F Mattei, M G Mattei, et al.
Page
of 30
Search research articles
Search
Showing results (71-80 of 295) with videos related to
Sort By:
Page
of 30
Human Genetics
|
January 19, 1979
Origin of the extra chromosome in trisomy 21
J F Mattei, M G Mattei, S Ayme, et al.
Human Genetics
|
January 1, 1981
Partial inversion of the secondary constriction of chromosome 9. Does it exist?
M G Mattei, J F Mattei, M Guichaoua, et al.
Human Genetics
|
January 1, 1981
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approach
M G Mattei, J F Mattei, I Vidal, et al.
Pediatrie
|
July 1, 1971
[Lyell syndrome and its sequelae in an asthmatic child]
E Louchet, L A Gratecos, C Paoli, et al.
Clinical Genetics
|
September 1, 1983
Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletion
J F Mattei, M G Mattei, P Balestrazzi, et al.
Journal De Genetique Humaine
|
March 1, 1982
[Interstitial deletion of chromosome 7 (7q33 to q35)]
M Arnolds, M G Mattei, P Rebuffel, et al.
Human Genetics
|
January 1, 1982
X-autosome translocations: cytogenetic characteristics and their consequences
M G Mattei, J F Mattei, S Ayme, et al.
Human Genetics
|
September 2, 1979
Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation
M G Mattei, J F Mattei, R Bernard, et al.
Human Genetics
|
October 28, 1976
Constitutional chromosomal breakage
F Giraud, S Ayme, J F Mattei, et al.
Humangenetik
|
August 25, 1975
[Partial trisomy 11q and familial translocation 11--22 (author's transl)]
F Giraud, J F Mattei, M G Mattei, et al.
Page
of 30