Inactivation pattern of the fragile X in heterozygous carriers
暂无分享,去创建一个
H. Berghe | J. Fryns | A. Kleczkowska | P. Petit | E. Kubień
[1] H. van den Berghe,et al. Inactivation pattern of the fragile X in heterozygous carriers. , 1989, Human genetics.
[2] J. Knoll,et al. Fragile (X) X-linked mental retardation. II. Frequency and replication pattern of fragile (X)(q28) in heterozygotes. , 1984, American journal of human genetics.
[3] N. Tommerup,et al. Carrier detection and X-inactivation studies in the fragile X syndrome , 1983, Human Genetics.
[4] I. Uchida,et al. Activity of the fragile X in heterozygous carriers. , 1982, American journal of human genetics.
[5] G. Sutherland. Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium. , 1977, Science.
[6] A. Hagemeijer,et al. Late-replicating ring X-chromosomes identified by r-banding after BrdU pulse , 1976, Human Genetics.
[7] U. Froster-Iskenius,et al. Screening for fra(X)(q) in a population of mentally retarded males , 2004, Human Genetics.
[8] P. Jacobs,et al. A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome , 2004, Human Genetics.
[9] U. Froster-Iskenius,et al. Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q) , 2004, Human Genetics.
[10] J. Fryns. The female and the fragile X. A study of 144 obligate female carriers. , 1986, American journal of medical genetics.
[11] P. Jacobs,et al. X-linked mental retardation: a study of 7 families. , 1980, American journal of medical genetics.
[12] D. S. Herbst. Nonspecific X-linked mental retardation I: a review with information from 24 new families. , 1980, American journal of medical genetics.