NOTES ON CLINICAL FEATURES OF A 46, XXP-PATIENTISHITOBI K; NAKADA N; WATANABE A et al.1982; PROCEEDINGS OF THE JAPAN ACADEMY. SERIES B: PHYSICAL AND BIOLOGICAL SCIENCES; ISSN 0386-2208; JPN; DA. 1982; VOL. 63; NO 2; PP. 25-28; BIBL. 10 REF.Article

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INHERITED PARTIAL X CHROMOSOME DUPLICATION IN A MENTALLY RETARDED MALENIELSEN KB; LANGKAER F.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 3; PP. 222-236; BIBL. 9 REF.Article

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