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J-F Mattei

Showing results (121-130 of 202) with videos related to

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Pediatrie|June 1, 1972
[Survey on the transmission of glucose-6-phosphate dehydrogenase deficiency. Study apropos of 34 families including 86 enzymopenic patients]A Orsini, L Vovan, Y Brusquet, et al.
Pathologie-Biologie|October 1, 1979
[Thrombopenia and radial aplasia: 2 cases with platelet function and ultrastructural studies of megakaryocytes and platelets (author's transl)]I Juhan, J Bayle, J F Mattei, et al.
Genetical Research|June 1, 1989
Chromosomal localization of the mouse gene coding for vimentinM 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.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|February 18, 1980
[Thrombopenia and radial aplasia: 2 cases with platelet function and ultrastructural studies of megakaryocytes and platelets (author's transl)]I Juhan, J Bayle, J F Mattei, et al.
European Journal of Pediatrics|February 1, 1988
The acrocallosal syndromeN Philip, N Apicella, I Lassman, et al.
American Journal of Medical Genetics|February 1, 1991
Transmission of mental retardation with fragile X site by two normal transmitter brothersM C Pellissier, M A Voelckel, C Piquet, et al.
Human Genetics|August 31, 1977
A girl with mosaicism for a dicentric X chromosome (45,X/46,X,dic(X) (Xqter to p22::p22 to qter))J F Mattei, H Taramasco, M G Mattei, et al.
Archives Francaises De Pediatrie|May 1, 1972
[Value of fluorescence for the identification of human chromosomes]F Giraud, M G Mattei, M Harung, et al.
Hemoglobin|November 24, 1999
Characterization of a new polymorphism, IVS-I-108 (T-->C), and a new beta-thalassemia mutation, -27 (A-->T), discovered in the course of a prenatal diagnosisC Badens, N Jassim, N Martini, et al.
Pageof 21

Showing results (121-130 of 202) with videos related to

Sort By:
Pageof 21
Pediatrie|June 1, 1972
[Survey on the transmission of glucose-6-phosphate dehydrogenase deficiency. Study apropos of 34 families including 86 enzymopenic patients]A Orsini, L Vovan, Y Brusquet, et al.
Pathologie-Biologie|October 1, 1979
[Thrombopenia and radial aplasia: 2 cases with platelet function and ultrastructural studies of megakaryocytes and platelets (author's transl)]I Juhan, J Bayle, J F Mattei, et al.
Genetical Research|June 1, 1989
Chromosomal localization of the mouse gene coding for vimentinM 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.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|February 18, 1980
[Thrombopenia and radial aplasia: 2 cases with platelet function and ultrastructural studies of megakaryocytes and platelets (author's transl)]I Juhan, J Bayle, J F Mattei, et al.
European Journal of Pediatrics|February 1, 1988
The acrocallosal syndromeN Philip, N Apicella, I Lassman, et al.
American Journal of Medical Genetics|February 1, 1991
Transmission of mental retardation with fragile X site by two normal transmitter brothersM C Pellissier, M A Voelckel, C Piquet, et al.
Human Genetics|August 31, 1977
A girl with mosaicism for a dicentric X chromosome (45,X/46,X,dic(X) (Xqter to p22::p22 to qter))J F Mattei, H Taramasco, M G Mattei, et al.
Archives Francaises De Pediatrie|May 1, 1972
[Value of fluorescence for the identification of human chromosomes]F Giraud, M G Mattei, M Harung, et al.
Hemoglobin|November 24, 1999
Characterization of a new polymorphism, IVS-I-108 (T-->C), and a new beta-thalassemia mutation, -27 (A-->T), discovered in the course of a prenatal diagnosisC Badens, N Jassim, N Martini, et al.
Pageof 21