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Annales De Genetique|March 1, 1976
Deletion - translocation del (12) (p11) leads to (t10;12) (p13;pII)J Nielsen, K Rasmussen, E NiebuhrAnnales De Genetique|September 1, 1975
[Trial of detection of female carriers for the ornithine-carbamyltransferase deficiency by the urine assay of crotic acid. Apropos of a family study]J L Dhondt, J P FarriauxAnnales De Genetique|June 1, 1975
[Localization of the genes of 28S and 18S RNA in human somatic chromosomes by in situ hybridization]D Pardo, J M Luciani, A StahlAnnales De Genetique|June 1, 1975
Brachydactyly type B and symphalangism in different members of a Mexican familyC Zavala, J Hernández-Ortíz, R LiskerAnnales De Genetique|June 1, 1975
A case of ring 18 chromosome in a sibship with multiple spontaneous abortionsR Coco, C Z Barreiro, V B PenchaszadehAnnales De Genetique|October 20, 1999
Genetic comparisons of patients with cystic fibrosis with or without meconium ileus. Clinical Centers of the French CF RegistryJ Feingold, M Guilloud-BatailleAnnales De Genetique|October 20, 1999
Pure partial trisomy 5q33-->5q35 resulting from the adjacent-1 segregation of a paternal (5;14)(q33;p12) translocationA Paoloni-Giacobino, A Bottani, S P DahounAnnales De Genetique|August 6, 1999
Probing the human genome in search for a new 3q syndromeG M Azar, R A Conte, S M Kleyman, et al.Annales De Genetique|February 16, 2000
A survey of fragile X syndrome in a sample from Spanish Basque countryI Arrieta, B Criado, B Martinez, et al.Pageof 129