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F Mattei

Showing results (121-130 of 295) with videos related to

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Clinical Genetics|February 1, 1980
Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1J F Mattei, M G Mattei, J P Ardissone, et al.
The Journal of Heart Transplantation|September 1, 1985
Heart transplantation in Paris, at "La Pitie" HospitalC Cabrol, I Gandjbakhch, A Pavie, et al.
Marseille Medical|January 1, 1971
[Congenital tuberculosis of bronchopneumonic form]E Louchet, A Orsini, J C Dieu, et al.
Pediatrie|June 1, 1975
[The chromosome 13 in ring syndrome]F Giraud, J M Emberger, N Pinsard, et al.
Annales De Chirurgie Thoracique Et Cardio-Vasculaire|October 1, 1975
[The surgical cure of aneurysms of the brachio-cephalic arterial trunk (author's transl)]G Escande, I Gandjbakhch, C Christides, et al.
Journal De Genetique Humaine|January 1, 1988
[Balanced chromosome rearrangements with abnormal phenotype]N Philip, M G Mattei, M C Pellissier, et al.
Biology of the Cell|January 1, 1989
Chromosomal localization of the mouse gene coding for the 68 kDa neurofilament subunitM G Mattei, P Duprey, Z L Li, et al.
Acta Paediatrica Scandinavica|September 1, 1985
Immunoreactive SOD-1 in amniotic fluid, amniotic cells and fibroblasts from trisomy 21 fetusM A Baeteman, M G Mattei, A Baret, et al.
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 syndromeI Oberlé, J L Mandel, J Boué, et al.
Pageof 30

Showing results (121-130 of 295) with videos related to

Sort By:
Pageof 30
Clinical Genetics|February 1, 1980
Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1J F Mattei, M G Mattei, J P Ardissone, et al.
The Journal of Heart Transplantation|September 1, 1985
Heart transplantation in Paris, at "La Pitie" HospitalC Cabrol, I Gandjbakhch, A Pavie, et al.
Marseille Medical|January 1, 1971
[Congenital tuberculosis of bronchopneumonic form]E Louchet, A Orsini, J C Dieu, et al.
Pediatrie|June 1, 1975
[The chromosome 13 in ring syndrome]F Giraud, J M Emberger, N Pinsard, et al.
Annales De Chirurgie Thoracique Et Cardio-Vasculaire|October 1, 1975
[The surgical cure of aneurysms of the brachio-cephalic arterial trunk (author's transl)]G Escande, I Gandjbakhch, C Christides, et al.
Journal De Genetique Humaine|January 1, 1988
[Balanced chromosome rearrangements with abnormal phenotype]N Philip, M G Mattei, M C Pellissier, et al.
Biology of the Cell|January 1, 1989
Chromosomal localization of the mouse gene coding for the 68 kDa neurofilament subunitM G Mattei, P Duprey, Z L Li, et al.
Acta Paediatrica Scandinavica|September 1, 1985
Immunoreactive SOD-1 in amniotic fluid, amniotic cells and fibroblasts from trisomy 21 fetusM A Baeteman, M G Mattei, A Baret, et al.
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 syndromeI Oberlé, J L Mandel, J Boué, et al.
Pageof 30