No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers [1]

American Journal of Human Genetics

Volumn 67, Issue 1, 2000, Pages 253-254

  Murray, A ^a   Ennis, S ^a   Morton, N ^a  

^a SALISBURY DISTRICT HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; COHORT ANALYSIS; DISEASE CLASSIFICATION; DISEASE TRANSMISSION; FEMALE; FRAGILE X SYNDROME; HUMAN; LETTER; MAJOR CLINICAL STUDY; MARKER GENE; MENOPAUSE; MENSTRUAL CYCLE; MUTATION; OVARY DISEASE; PRIORITY JOURNAL; SURVIVAL;

EID: 0033926935     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302963     Document Type: Letter

References (4)

1. RDL Hundscheid EA Sistermans CMG Thomas DDM Braat H Straatman LALM Kiemeney BA Oostra Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations Am J Hum Genet 66 2000 413 418
2. NE Morton JN Macpherson Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus Proc Natl Acad Sci USA 89 1992 4215 4217
3. Murray A, Ennis S, MacSwiney F, Webb J, Morton N. Reproductive and menstrual history of females with fragile X expansions. Eur J Hum Genet (in press)
4. A Murray J Webb S Grimley G Conway P Jacobs Studies of FRAXA and FRAXE in women with premature ovarian failure J Med Genet 35 1998 637 640