CHOANAL ATRESIA AND ASSOCIATED MULTIPLE ANOMALIESHALL BD.1979; J. PEDIATR.; USA; DA. 1979; VOL. 95; NO 3; PP. 395-398; BIBL. 7 REF.Article

MENTAL RETARDATION AND MULTIPLE CONGENITAL ANOMALIES OF UNKNOWN ETIOLOGY: FREQUENCY OF OCCURRENCE IN SIMILARLY AFFECTED SIBS OF THE PROBANDBARTLEY JA; HALL BD.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6B; PP. 127-137; BIBL. 1 REF.Article

TRANSCRIPTION IN YEAST: ALPHA -AMANITIN SENSITURTY AND OTHER PROPERTIES WHICH DISTINGUISH BETWEEN RNA POLYMERASES I AND III.SCHULTZ LD; HALL BD.1976; PROC. NATION. ACAD. SCI. U.S.A.; U.S.A.; DA. 1976; VOL. 73; NO 4; PP. 1029-1033; BIBL. 31 REF.Article

CODON SELECTION IN YEASTBENNETZEN JL; HALL BD.1982; J. BIOL. CHEM.; ISSN 0021-9258; USA; DA. 1982; VOL. 257; NO 6; PP. 3026-3031; BIBL. 47 REF.Article

THE PRIMARY STRUCTURE OF THE SACCHAROMYCES CEREVISIAE GENE FOR ALCOHOL DEHYDROGENASE 1BENNETZEN JL; HALL BD.1982; J. BIOL. CHEM.; ISSN 0021-9258; USA; DA. 1982; VOL. 257; NO 6; PP. 3018-3025; BIBL. 37 REF.Article

ETIOLOGIC FACTORS IN THE AMNIOTIC BAND SYNDROME: A STUDY OF 24 PATIENTS.OSSIPOFF V; HALL BD.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3D; PP. 117-132; BIBL. 39 REF.Article

THE PRIMARY STRUCTURE OF THE ALCOHOL DEHYDROGENASE GENE FROM THE FISSION YEAST SCHIZOSACCHAROMYCES POMBERUSSELL PR; HALL BD.1983; JOURNAL OF BIOLOGICAL CHEMISTRY; ISSN 0021-9258; USA; DA. 1983; VOL. 258; NO 1; PP. 143-149; BIBL. 34 REF.Article

CHARACTERIZATION OF THE YEAST TRNA₂^SER GENE FAMILY: GENOMIC ORGANIZATION AND DNA SEQUENCEPAGE GS; HALL BD.1981; NUCLEIC ACIDS RES.; ISSN 0305-1048; GBR; DA. 1981; VOL. 9; NO 4; PP. 921-934; BIBL. 28 REF.Article

THE COFFIN-SIRIS SYNDROMECAREY JC; HALL BD.1978; AMER. J. DIS. CHILD.; USA; DA. 1978; VOL. 132; NO 7; PP. 667-671; BIBL. 6 REF.Article

YEAST CYTOCHROME C MESSENGER RNA. IN VITRO TRANSLATION AND SPECIFIC IMMUNOPRECIPITATION OF THE CYCL GENE PRODUCT.ZITOMER RS; HALL BD.1976; J. BIOL. CHEM.; U.S.A.; DA. 1976; VOL. 251; NO 20; PP. 6320-6326; BIBL. 31 REF.Article

PRADER-WILLI SYNDROME = SYNDROME DE PRADER-WILLIHALL BD; SMITH DW.1972; J. PEDIATR.; U.S.A.; DA. 1972; VOL. 81; NO 2; PP. 286-293; BIBL. 12REF.Article

PENETRANCE AND VARIABILITY IN NEUROFIBROMATOSIS: A GENETIC STUDY OF 60 FAMILIESCAREY JC; LAUB JM; HALL BD et al.1979; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1979; VOL. 15; NO 5B; PP. 271-281; BIBL. 12 REF.Article

THE OEIS COMPLEX (OMPHALOCELE, EXSTROPHY, IMPERFORATE ANUS, SPINAL DEFECTS)CAREY JC; GREENBAUM B; HALL BD et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6B; PP. 253-263; BIBL. 32 REF.Article

A YEAST MUTANT DEFECTIVE IN THE PROCESSING OF 27S R-RNA PRECURSORANDREW C; HOPPER AK; HALL BD et al.1976; MOLEC. GEN. GENET.; GERM.; DA. 1976; VOL. 144; NO 1; PP. 29-37; BIBL. 15 REF.Article

THE AARSKOG SYNDROMEFURUKAWA CT; HALL BD; SMITH DW et al.1972; J. PEDIATR.; U.S.A.; DA. 1972; VOL. 81; NO 6; PP. 1117-1122; BIBL. 15 REF.Serial Issue

TRANSCRIPTION IN YEAST: SEPARATION AND PROPERTIES OF MULTIPLE RNA POLYMERASESADMAN R; SCHULTZ LD; HALL BD et al.1972; PROC. NATION. ACAD. SCI. U.S.A.; U.S.A.; DA. 1972; VOL. 69; NO 7; PP. 1702-1706; BIBL. 27REF.Serial Issue

MATING TYPE AND SPORULATION IN YEAST. II. MEIOSIS, RECOMBINATION, AND RADIATION SENSITIVITY IN AN ALPHA ALPHA DIPLOID WITH ALTERED SPORULATION CONTROL. V.HOPPER AK; KIRSCH J; HALL BD et al.1975; GENETICS; U.S.A.; DA. 1975; VOL. 80; NO 1; PP. 61-76; BIBL. 1 P. 1/2Article

BRIEF CLINICAL REPORT: A NEW SYNDROME OF HEMANGIOMATOUS BRANCHIAL CLEFTS, LIP PSEUDOCLEFTS, AND UNUSUAL FACIAL APPEARANCEHALL BD; DELORIMIER A; FOSTER LH et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 1; PP. 135-138; BIBL. 4 REF.Article

GENETIC ANALYSIS OF THE PROCESSING OF A SPLICED TRNANISHIKURA K; KURJAN J; HALL BD et al.1982; EMBO J.; ISSN 503827; GBR; DA. 1982; VOL. 1; NO 2; PP. 263-268; BIBL. 37 REF.Article

THE AMNIOTIC BAND DISRUPTION COMPLEX: TIMING OF AMNIOTIC RUPTURE AND VARIABLE SPECTRA OF CONSEQUENT DEFECTSHIGGINBOTTOM MC; JONES KL; HALL BD et al.1979; J. PEDIATR.; USA; DA. 1979; VOL. 95; NO 4; PP. 544-549; BIBL. 9 REF.Article

PRENATAL DIAGNOSIS OF ACHONDROGENESIS.GOLBUS MS; HALL BD; FILLY RA et al.1977; J. PEDIATR.; U.S.A.; DA. 1977; VOL. 91; NO 3; PP. 464-466; BIBL. 17 REF.Article

DUPLICATION (PARTIAL TRISOMY) OF THE DISTAL LONG ARM OF CHROMOSOME 17: A NEW CLINICALLY RECOGNIZABLE CHROMOSOME DISORDERBERBERICH MS; CAREY JC; LAWCE HJ et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 287-295; BIBL. 3 REF.Article

DELETION MAPPING OF SEQUENCES ESSENTIAL FOR IN VIVO TRANSCRIPTION OF THE ISO-1 CYTOCHROME C GENEFAYE G; LEUNG DW; TATCHELL K et al.1981; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1981; VOL. 78; NO 4; PP. 2258-2262; BIBL. 28 REF.Article

CLONING OF THE YEAST TYROSINE TRANSFER RNA GENES IN BACTERIOPHAGE LAMBDAOLSON MV; HALL BD; CAMERON JR et al.1979; J. MOLEC. BIOL.; GBR; DA. 1979; VOL. 127; NO 3; PP. 285-295; BIBL. 30 REF.Article

FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME = SYNDROME HYPOPLASIE FEMORALE-FACIES INHABITUELDAENTL DL; SMITH DW; SCOTT CI et al.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 86; NO 1; PP. 107-111; BIBL. 4REF.Article