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Annales De Genetique|June 1, 1977
[Two new cases of trisomy 10q21 to 10qter in two sisters due to paternal translocation t(9;10) (q34;q24)]J Fraisse, B Lauras, A La Selve, et al.Annales De Genetique|October 20, 1999
Familial high myopia: evidence of an autosomal dominant mode of inheritance and genetic heterogeneityL Naiglin, J Clayton, C Gazagne, et al.Annales De Genetique|February 16, 2000
A novel and very peculiar HincII polymorphism in the 5' region of the human neurofibromatosis type 1 (NF1) geneL J Fang, J Feingold, B Lemieux, et al.Annales De Genetique|October 20, 1999
CTG instability in myotonic dystrophy: molecular genetic analysis of families from south-eastern France with characteristics of intergenerational variation in CGT repeat numbersS Duthel, M Bost, E Ollagnon, et al.Annales De Genetique|October 20, 1999
Familial coarctation of the aorta in three generationsC Stoll, Y Alembik, B DottAnnales De Genetique|August 6, 1999
Growth curves of children with Down syndromeC Toledo, Y Alembik, A Aguirre Jaime, et al.Annales De Genetique|August 6, 1999
A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)T Lukusa, K Devriendt, J P FrynsAnnales De Genetique|August 6, 1999
Cri du chat and Turner syndrome features in a newborn girl with an unbalanced 45,X,psu dic(5;X)(p15.2;p22.1) karyotype: FISH and replication banding studiesK S Reddy, D L Smith, C S BallAnnales De Genetique|September 22, 2000
Human TIP49b/RUVBL2 gene: genomic structure, expression pattern, physical link to the human CGB/LHB gene cluster on chromosome 19q13.3B Parfait, Y Giovangrandi, M Asheuer, et al.Annales De Genetique|September 22, 2000
The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populationsI P Dávalos, N Olivares, M T Castillo, et al.Pageof 129