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Volumn 84, Issue 3, 1999, Pages 202-203
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Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology [2]
a
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Author keywords
[No Author keywords available]
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Indexed keywords
CHILD;
DISEASE ASSOCIATION;
FEMALE;
FRAGILE X SYNDROME;
GENE MUTATION;
HIGH RISK POPULATION;
HUMAN;
LETTER;
MAJOR CLINICAL STUDY;
MALE;
MASS SCREENING;
MENTAL DEFICIENCY;
MUTATION RATE;
POLYMERASE CHAIN REACTION;
PREVALENCE;
PRIORITY JOURNAL;
TRINUCLEOTIDE REPEAT;
TURKEY (REPUBLIC);
ADOLESCENT;
CHILD;
CHILD, PRESCHOOL;
FEMALE;
FRAGILE X SYNDROME;
GENETIC SCREENING;
HUMANS;
MALE;
MENTAL RETARDATION;
TURKEY;
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EID: 0033612339
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/(SICI)1096-8628(19990528)84:3<202::AID-AJMG6>3.0.CO;2-O Document Type: Letter |
Times cited : (11)
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References (5)
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