000 01580 a2200457 4500
005 20250515053315.0
264 0 _c20070301
008 200703s 0 0 eng d
022 _a1098-3600
024 7 _a10.1097/gim.0b013e31802d833c
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aStrom, Charles M
245 0 0 _aMolecular testing for Fragile X Syndrome: lessons learned from 119,232 tests performed in a clinical laboratory.
_h[electronic resource]
260 _bGenetics in medicine : official journal of the American College of Medical Genetics
_cJan 2007
300 _a46-51 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aFemale
650 0 4 _aFragile X Mental Retardation Protein
_xgenetics
650 0 4 _aFragile X Syndrome
_xdiagnosis
650 0 4 _aGene Frequency
650 0 4 _aGenetic Counseling
650 0 4 _aGenetic Testing
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aLaboratories
650 0 4 _aMale
650 0 4 _aPrenatal Diagnosis
650 0 4 _aTrinucleotide Repeat Expansion
700 1 _aCrossley, Beryl
700 1 _aRedman, Joy B
700 1 _aBuller, Arlene
700 1 _aQuan, Franklin
700 1 _aPeng, Mei
700 1 _aMcGinnis, Matthew
700 1 _aFenwick, Raymond G
700 1 _aSun, Weimin
773 0 _tGenetics in medicine : official journal of the American College of Medical Genetics
_gvol. 9
_gno. 1
_gp. 46-51
856 4 0 _uhttps://doi.org/10.1097/gim.0b013e31802d833c
_zAvailable from publisher's website
999 _c16789362
_d16789362