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HUMAN NEUTRAL ALPHA -GLUCOSIDASE C: GENETIC POLYMORPHISM INCLUDING A "NULL" ALLELEMARTINIUK F; HIRSCHHORN R.1980; AMER. J. HUM. GENET.; USA; DA. 1980; VOL. 32; NO 4; PP. 497-507; BIBL. 31 REF.Article

EVIDENCE FOR A NULL ALLELE AT THE ESTERASE D (EC 3.1.1.1) LOCUSSPARKES RS; TARGUM S; GERSHON E et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 319-323; BIBL. 4 REF.Article

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A TYPICAL SEGREGATION OF ESTERASE D: EVIDENCE OF A RARE "SILENT" ALLELE ESD^OKOZIOL P; STEPIEN J.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 223-225; BIBL. 11 REF.Article

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LE DEFICIT EN ALPHA-1-ANTITRYPSINE ET L'ALLELE PI NULMARTIN JP; ROPARTZ C.1975; REV. FR. TRANSFUS. IMMUNO-HEMATOL.; FR.; DA. 1975; VOL. 18; NO 1; PP. 27-45; ABS. ANGL.; BIBL. 2 P.Article

UEBER DAS VORKOMMEN DES STUMMEN ALLELS P^O IN 10 DEUTSCHEN FAMILIEN = SUR L'APPARITION DE L'ALLELE MUET P^O DANS 10 FAMILLES ALLEMANDESBRINKMANN B; HOPPE HH; SACHS HW et al.1974; Z. RECHTSMED.; DTSCH.; DA. 1974; VOL. 75; NO 1; PP. 25-32; ABS. ANGL.; BIBL. 15 REF.Article

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DETECTION OF HB-PAPIO B, A SILENT MUTATION OF THE BABOON BETA CHAIN, BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY: IMPROVED PROCEDURES FOR THE SEPARATION OF GLOBIN CHAINS BY HPLCSHELTON JB; SHELTON JR; SCHROEDER WA et al.1982; HEMOGLOBIN; ISSN 0363-0269; USA; DA. 1982; VOL. 6; NO 5; PP. 451-464; BIBL. 13 REF.Article

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FY (A-B-) PHENOTYPE IN CZECHOSLOVAKIALIBICH M; KOUT M; GILES CM et al.1978; VOX SANG.; CHE; DA. 1978; VOL. 35; NO 6; PP. 423-425; BIBL. 10 REF.Article

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