Showing results (791-800 of 6,484) with videos related to
Sort By:
Pageof 649
Journal of Medical Genetics|January 1, 1990
De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomaliesI K Temple, J A Hurst, S Hing, et al.Journal of Medical Genetics|August 16, 2012
Miglustat as a therapeutic agent: prospects and caveatsRosemarie E Venier, Suleiman A IgdouraJournal of Medical Genetics|August 1, 1979
Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter)A Daniel, T Saville, D B SouthallJournal of Medical Genetics|June 1, 1975
Amniotic fluid macrophages and the antenatal diagnosis of anencephaly and spina bifidaG R Sutherland, D J Brock, J B ScrimgeourJournal of Medical Genetics|June 1, 1975
A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)]C KempenJournal of Medical Genetics|July 25, 1998
Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomesT Yorifuji, J Muroi, M Kawai, et al.Journal of Medical Genetics|July 25, 1998
Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibsD Wieczorek, H Engels, R Viersbach, et al.Journal of Medical Genetics|July 25, 1998
Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of ScotlandW K Lee, L Haddad, M J Macleod, et al.Journal of Medical Genetics|July 25, 1998
Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPPE Nelis, P De Jonghe, E De Vriendt, et al.Pageof 649