Between-generation differences in ascertainment and penetrance: relevance to genetic hypotheses in fragile X
- 1 June 1993
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 91 (5) , 469-474
- https://doi.org/10.1007/bf00217774
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Experience with direct molecular diagnosis of fragile X.Journal of Medical Genetics, 1992
- Problems in ascertainment of transmitting males in Martin‐Bell syndromeAmerican Journal of Medical Genetics, 1991
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Neuropsychological dimensions of the fragile X syndrome: Support for a non-dominant hemisphere dysfunction hypothesisNeuropsychologia, 1990
- Clinical features and reproductive patterns in fragile X female heterozygotes.Journal of Medical Genetics, 1988
- Anthropometry in Martin‐Bell syndromeAmerican Journal of Medical Genetics, 1988
- The fragile X syndrome in a large family. I. Cytogenetic and clinical investigations.Journal of Medical Genetics, 1987
- Twelve families with fragile X(q27).Journal of Medical Genetics, 1986
- Further segregation analysis of the fragile X syndrome with special reference to transmitting malesHuman Genetics, 1985
- The marker (X) syndrome: a cytogenetic and genetic analysisAnnals of Human Genetics, 1984