Published in Hum Genet on February 01, 1980
FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition. Am J Hum Genet (1981) 2.09
Activity of the fragile X in heterozygous carriers. Am J Hum Genet (1982) 2.06
5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardation. J Med Genet (1981) 1.24
Fragile X chromosome: clinical and cytogenetic studies on cases from seven families. J Med Genet (1983) 1.20
Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25, 16q22, and 17p12. Am J Hum Genet (1984) 0.95
The fragile X syndrome: the patients and their chromosomes. J Med Genet (1984) 0.83
Fragile X syndrome: search for phenotypic manifestations at loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase. Am J Hum Genet (1981) 0.82
Intracellular folate distribution in cultured fibroblasts from patients with the fragile X syndrome. Am J Hum Genet (1983) 0.79
X-linked mental retardation. Arch Dis Child (1981) 0.78
Inducing fragile sites to express themselves. Am J Hum Genet (1980) 0.77
Thymidylate synthetase inhibitors and fragile site expression in lymphocytes. Am J Hum Genet (1983) 0.75
A comparison of fragile X expression in lymphocyte and lymphoblastoid cultures. Am J Hum Genet (1986) 0.75
Fragile X-linked mental retardation of macro-orchidism. West J Med (1982) 0.75
Chromosomal mosaicism confined to the placenta in human conceptions. Science (1983) 1.67
Cytogenetic evaluation of four canine mast cell tumors. Cancer Genet Cytogenet (1991) 1.40
Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation. J Med Genet (1993) 1.30
CFU-S in individual erythroid colonies derived in vitro from adult mouse marrow. Nature (1979) 1.17
Klinefelter's syndrome and acute leukemia. Cancer Genet Cytogenet (1987) 1.07
Confined chorionic mosaicism in prenatal diagnosis. Hum Genet (1987) 1.02
Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome). Am J Med Genet (1986) 1.00
A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome. J Med Genet (1970) 0.98
Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation. Hum Mol Genet (1999) 0.97
Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25, 16q22, and 17p12. Am J Hum Genet (1984) 0.95
Nondisjunction in aging female mice. Cytogenet Cell Genet (1976) 0.94
Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23. Am J Hum Genet (1983) 0.93
Placental morphology in spontaneous human abortuses with normal and abnormal karyotypes. Teratology (1976) 0.91
Fragile sites in chromosomes: possible model for the study of spontaneous chromosome breakage. Science (1983) 0.88
The fragile X chromosome: current methods. Am J Med Genet (1982) 0.87
Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect. Am J Hum Genet (1999) 0.86
Characterization of an inversion duplication of the short arm of chromosome 8 by fluorescent in situ hybridization. Am J Med Genet (1992) 0.85
X chromosome aneuploidy in lymphocyte cultures from women with recurrent spontaneous abortions. Am J Med Genet (1987) 0.84
Embryonic development in ectopic human pregnancy. Teratology (1976) 0.84
Further delineation of X-linked mental retardation. Hum Genet (1981) 0.83
Two kinships with accessory bisatellited chromosomes. Ann Genet (1973) 0.82
Ring 13 chromosome associated with microcephaly, congenital heart defect, intrauterine growth retardation, and abnormal skin pigmentation. Birth Defects Orig Artic Ser (1977) 0.81
Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2. Am J Med Genet (1998) 0.80
Triploidy in 40 human spontaneous abortuses: assessment of phenotype in embryos. Obstet Gynecol (1981) 0.79
Chromosomal fragile site expression in dogs: II. Expression in boxer dogs with mast cell tumors. Am J Med Genet (1991) 0.78
Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype. Am J Med Genet (1993) 0.77
Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10. Genomics (1992) 0.77
Chromosomal fragile site expression in dogs: I. Breed specific differences. Am J Med Genet (1991) 0.77
The giemsa banding pattern of canine chromosomes, using a cell synchronization technique. Genome (1991) 0.75
Thymidylate synthetase inhibitors and fragile site expression in lymphocytes. Am J Hum Genet (1983) 0.75
Rapid determination of polyploidy in human chorionic tissue sections. Hum Genet (1977) 0.75
Infantile autism: an occasional manifestation of fragile (X) mental retardation. Am J Med Genet (1986) 0.75
Interferon-inducible fragile site on chromosome 16. Lancet (1981) 0.75
A hitherto undescribed chromosome structural anomaly in a mentally retarded child. Ann Hum Genet (1966) 0.75
A novel Robertsonian translocation in a family of Walker hounds. Genome (1991) 0.75
Dictyotene Stage of Meiosis in Mosses. Science (1964) 0.75
FMC-HU-1-B: a lymphoma B-cell line with unusual characteristics. Leuk Res (1985) 0.75
The association of hydatidiform mole and trisomy 2. Obstet Gynecol (1974) 0.75
Prenatal diagnosis of chromosomal mosaicism for trisomy D. J Pediatr (1977) 0.75
Fragile X chromosome and chromosome condensation. Ann Genet (1983) 0.75