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Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family
Author(s) -
Anvret Maria,
Gillberg Christopher,
Wahlström Jan,
AlbertssonWikland Kerstin,
Davies Kay
Publication year - 1988
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1988.tb02874.x
Subject(s) - fragile x syndrome , autism , fragile x , genetics , restriction fragment length polymorphism , genetic linkage , x chromosome , biology , linkage (software) , chromosomal fragile site , psychology , developmental psychology , genotype , gene , chromosome
In an extended family with eight individuals with infantile autism, in association with other developmental disorders and fragile (X) (q27.3), DNA techniques were used to investigate linkage between X chromosomal probes and the disorder. F9 was not informative and recombination was found between fragile X and DXS15, DXS51 and DXS52.