000 01318 a2200337 4500
005 20250513233352.0
264 0 _c20010426
008 200104s 0 0 eng d
022 _a1098-3600
024 7 _a10.1097/00125817-200007000-00007
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBurman, R W
245 0 0 _aFragile X full mutations are more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics.
_h[electronic resource]
260 _bGenetics in medicine : official journal of the American College of Medical Genetics
_c
300 _a242-8 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aBlotting, Southern
650 0 4 _aFamily Health
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aGenetic Variation
650 0 4 _aHumans
650 0 4 _aModels, Statistical
650 0 4 _aMutation
650 0 4 _aNuclear Family
650 0 4 _aPedigree
650 0 4 _aTrinucleotide Repeats
700 1 _aAnoe, K S
700 1 _aPopovich, B W
773 0 _tGenetics in medicine : official journal of the American College of Medical Genetics
_gvol. 2
_gno. 4
_gp. 242-8
856 4 0 _uhttps://doi.org/10.1097/00125817-200007000-00007
_zAvailable from publisher's website
999 _c11189430
_d11189430