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Medline ® Abstract for Reference 35

of 'Clinical manifestations and evaluation of spontaneous primary ovarian insufficiency (premature ovarian failure)'

35
TI
Fragile X syndrome: diagnostic and carrier testing.
AU
Sherman S, Pletcher BA, Driscoll DA
SO
Genet Med. 2005;7(8):584.
 
This guideline is designed primarily as an educational resource for medical geneticists and other health care providers to help them provide quality medical genetic services. Adherence to this guideline does not necessarily assure a successful medical outcome. This guideline should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. In determining the propriety of any specific procedure or test, the geneticist should apply his or her own professional judgment to the specific clinical circumstances presented by the individual patient or specimen. It may be prudent, however, to document in the patient's record the rationale for any significant deviation from this guideline.
AD
ACMG Professional Practice and Guidelines Committee, Emory University, Atlanta, Georgia, USA.
PMID