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Results: 1-2 |
Results: 2
PHENOTYPE-GENOTYPE CORRELATION IN 27 DELETION AND 27 NON DELETION ANGELMAN-SYNDROME PATIENTS - EVIDENCE OF A MILDER PHENOTYPE ASSOCIATED WITH NONDELETION AS PATIENTS
Authors: MONCLA A MALZAC P VOELCKEL MA GIRARDOT L MATTEI MG PHILIP N MATTEI JF LIVET MO
Citation: A. Moncla et al., PHENOTYPE-GENOTYPE CORRELATION IN 27 DELETION AND 27 NON DELETION ANGELMAN-SYNDROME PATIENTS - EVIDENCE OF A MILDER PHENOTYPE ASSOCIATED WITH NONDELETION AS PATIENTS, European journal of human genetics, 6, 1998, pp. 1065-1065
ATYPICAL MOLECULAR FINDINGS IDENTIFY LIMITS OF TECHNICAL SCREENING-TESTS FOR PRADER-WILLI AND ANGELMAN SYNDROME DIAGNOSES
Authors: MALZAC P MONCLA A PEDEILLIER K VAN CV GIRARDOT L VOELCKEL MA
Citation: P. Malzac et al., ATYPICAL MOLECULAR FINDINGS IDENTIFY LIMITS OF TECHNICAL SCREENING-TESTS FOR PRADER-WILLI AND ANGELMAN SYNDROME DIAGNOSES, American journal of medical genetics, 78(3), 1998, pp. 242-244
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