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Human Genetics|October 1, 1988
Mapping of the human retinoic acid receptor to the q21 band of chromosome 17M G Mattei, M Petkovich, J F Mattei, et al.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.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.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.European Journal of Pediatrics|January 1, 1984
Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13)J L Bernard, M A Baeteman, J F Mattei, et al.Nature|December 15, 1983
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal maleG 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 8pJ F Mattei, M G Mattei, J P Ardissone, et al.Pageof 14