| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/(SICI)1096-8628(19960809)64:2<256::AID-AJMG4>3.0.CO;2-S |
| P698 | PubMed publication ID | 8844059 |
| P2093 | author name string | Sherman SL | |
| Ashley AE | |||
| Meadows KL | |||
| P2860 | cites work | Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox | Q28235115 |
| Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation | Q33594670 | ||
| Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation | Q39111532 | ||
| Length of uninterrupted CGG repeats determines instability in the FMR1 gene | Q39111985 | ||
| Collaborative prospective study of the fragile X syndrome: request for participation | Q41182580 | ||
| Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects. | Q45290275 | ||
| Investigation of the twinning rate in families with the fragile X syndrome | Q45887973 | ||
| Affected sibs with fragile X syndrome exhibit an age-dependent decrease in the size of the fragile X full mutation | Q47397752 | ||
| Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles. | Q52025538 | ||
| Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion. | Q52035689 | ||
| Genotype mosaicism in fragile X fetal tissues | Q52044697 | ||
| The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm. | Q54047243 | ||
| Dizygous twinning and premature menopause in fragile X syndrome | Q57269215 | ||
| Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses | Q57732473 | ||
| Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development | Q57970194 | ||
| Precursor arrays for triplet repeat expansion at the fragile X locus | Q72449243 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 256-260 | |
| P577 | publication date | 1996-08-01 | |
| P1433 | published in | American Journal of Medical Genetics Part A | Q15755121 |
| P1476 | title | Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females | |
| P478 | volume | 64 |
| Q48788754 | Examination of reproductive aging milestones among women who carry the FMR1 premutation |
| Q35743415 | FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability |
| Q50623363 | Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers |
| Q35250296 | Fragile X premutations are not a major cause of early menopause |
| Q38542561 | Genetic Counseling for Fragile X Syndrome: Recommendations of the National Society of Genetic Counselors |
| Q36208811 | Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors |
| Q51999063 | Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X. |
| Q73929398 | Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes |
| Q57391840 | Is fragile X syndrome a risk factor for dizygotic twinning? |
| Q34306135 | Premature ovarian failure in the fragile X syndrome |
| Q37050992 | Reproductive and menstrual history of females with fragile X expansions |
| Q47236766 | Single nucleotide polymorphism and FMR1 CGG repeat instability in two Basque valleys. |
| Q39813107 | Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population |
| Q40793010 | Transcription of the FMR1 gene in individuals with fragile X syndrome |
Search more.