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Annales De Genetique
|
March 1, 1971
[46,XY-45,X mosaicism and 18p- deletion]
F Giraud, M Hartung, J F Mattei, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Dysmorphology report: on the association of microcephaly and preaxial polydactyly. Another example of Howard-Young syndrome
P Collignon, N Philip, G Simonin, et al.
Pediatrie
|
April 1, 1977
[Intra-erythrocytic enzyme activity in trisomy 21]
J F Mattei, L Vovan, S Ayme, et al.
Marseille Medical
|
January 1, 1971
[Limited epidemic of tuberculosis around a contaminator]
J Taranger, E Louchet, L A Gratecos-Trolliet, et al.
American Journal of Medical Genetics
|
January 1, 1982
GENTIC: a computerized medical genetic case record system
S Aymé, Y Aurran, J Gouvernet, et al.
Clinical Genetics
|
January 1, 1979
Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counselling
S Ayme, M G Mattei, J F Mattei, et al.
Cytogenetics and Cell Genetics
|
January 1, 1979
Distribution of spontaneous chromosome breaks in man
M G Mattei, S Ayme, J F Mattei, et al.
Pediatrie
|
October 1, 1978
[Severe hepatitis induced by chemotherapy with antitubercular agents in childhood. 2 cases]
P Chapoy, J P Ferracci, J F Mattei, et al.
Annales D'Endocrinologie
|
July 1, 1977
[46 XX karyotype men (author's transl)]
J Vague, J Guidon, J F Mattei, et al.
Life Sciences
|
February 21, 1983
Immunoreactive Cu-SOD and Mn-SOD in lymphocytes sub-populations from normal and trisomy 21 subjects according to age
M A Baeteman, A Baret, A Courtière, et al.
Page
of 21
Search research articles
Search
Showing results (81-90 of 202) with videos related to
Sort By:
Page
of 21
Annales De Genetique
|
March 1, 1971
[46,XY-45,X mosaicism and 18p- deletion]
F Giraud, M Hartung, J F Mattei, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Dysmorphology report: on the association of microcephaly and preaxial polydactyly. Another example of Howard-Young syndrome
P Collignon, N Philip, G Simonin, et al.
Pediatrie
|
April 1, 1977
[Intra-erythrocytic enzyme activity in trisomy 21]
J F Mattei, L Vovan, S Ayme, et al.
Marseille Medical
|
January 1, 1971
[Limited epidemic of tuberculosis around a contaminator]
J Taranger, E Louchet, L A Gratecos-Trolliet, et al.
American Journal of Medical Genetics
|
January 1, 1982
GENTIC: a computerized medical genetic case record system
S Aymé, Y Aurran, J Gouvernet, et al.
Clinical Genetics
|
January 1, 1979
Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counselling
S Ayme, M G Mattei, J F Mattei, et al.
Cytogenetics and Cell Genetics
|
January 1, 1979
Distribution of spontaneous chromosome breaks in man
M G Mattei, S Ayme, J F Mattei, et al.
Pediatrie
|
October 1, 1978
[Severe hepatitis induced by chemotherapy with antitubercular agents in childhood. 2 cases]
P Chapoy, J P Ferracci, J F Mattei, et al.
Annales D'Endocrinologie
|
July 1, 1977
[46 XX karyotype men (author's transl)]
J Vague, J Guidon, J F Mattei, et al.
Life Sciences
|
February 21, 1983
Immunoreactive Cu-SOD and Mn-SOD in lymphocytes sub-populations from normal and trisomy 21 subjects according to age
M A Baeteman, A Baret, A Courtière, et al.
Page
of 21