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Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4PINKEL, D; LANDEGENT, J; COLLINS, C et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 23, pp 9138-9142, issn 0027-8424Article

EVIDENCE FOR LOCALISATION OF GENES FOR HUMAN ALPHA -GLOBIN ON THE LONG ARM OF CHROMOSOME 4.GANDINI E; DALLAPICCOLA B; LAURENT C et al.1977; NATURE; G.B.; DA. 1977; VOL. 265; NO 5589; PP. 65-66; BIBL. 27 REF.Article

ASSOCIATION, CHEZ LE MEME SUJET, D'UNE DELETION DU BRAS COURT DU CHROMOSOME 4 (4P-) ET D'UN DEFICIT COMPLET EN PARAHYDROXYPHENYLPYRUVATE OXYDASE HEPATIQUE (TYROSINOSE)MALPUECH G; MATTEI JF; GAULME J et al.1981; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1981; VOL. 29; NO 4; PP. 455-461; ABS. ENG; BIBL. 8 REF.Article

Heteromorphic variants of human chromosome 4BABU, A; VERMA, R. S.Cytogenetics and cell genetics. 1986, Vol 41, Num 1, pp 60-61, issn 0301-0171Article

Suggested assignment of peptidase S (PEPS) to 4p11―4q12 by exclusion using gene dosage, accounting for variability in fibroblastsSCHMUTZ, S. M; SIMPSON, N. E.Human genetics. 1983, Vol 64, Num 2, pp 134-138, issn 0340-6717Article

ASSIGNMENT OF THE STRUCTURAL GENE CODING FOR ALBUMIN TO HUMAN CHROMOSOME 4FA TEN KAO; HAWKINS JW; LAW ML et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 4; PP. 337-341; BIBL. 34 REF.Article

Le syndrome trisomie pour la partie terminale du bras long du chromosome 4 = The 49 trisomy syndromeSTOLL, C; ROTH, M.-P; DOTT, B et al.Annales de pédiatrie (Paris). 1985, Vol 32, Num 6, pp 527-530, issn 0066-2097Article

A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressedKANG LI; WARNER, C. K; HODGE, J. A et al.The Journal of biological chemistry (Print). 1989, Vol 264, Num 24, pp 13998-14004, issn 0021-9258, 7 p.Article

Assignment of CD38, the gene encoding human leukocyte antigen CD38 (ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase), to chromosome 4p15NAKAGAWARA, K; MORI, M; OKAMOTO, H et al.Cytogenetics and cell genetics. 1995, Vol 69, Num 1-2, pp 38-39, issn 0301-0171Conference Paper

GENETIC LINKAGE DATA FOR THE DOMBROCK BLOOD GROUP LOCUS RELATIVE TO CHROMOSOME 1 AND CHROMOSOME 4 LOCILEWIS M; KAITA H; PHILIPPS S et al.1983; ANNALS OF HUMAN GENETICS; ISSN 0003-4800; GBR; DA. 1983; VOL. 47; NO 1; PP. 49-53; BIBL. 21 REF.Article

REGIONAL LOCALIZATION OF HUMAN PHOSPHOGLUCOMUTASE-2 LOCUS ON CHROMOSOME 4.SPARKES RS; MOHANDAS T; SPARKES MC et al.1978; EXPER. CELL RES.; U.S.A.; DA. 1978; VOL. 111; NO 2; PP. 492-495; BIBL. 7 REF.Article

THE WOLF-HIRSCHHORN (4P-) SYNDROME.JOHNSON VP; MULDER RD; HOSEN R et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 2; PP. 104-112; BIBL. 2 P.Article

LETTER TO THE EDITOR: DELETION OF CHROMOSOME 4Q33->QTER. IS IT DIFFERENT FROM 4Q31->QTER DELETION SYNDROME.TUCHMAN M; EBRAHIMI J; GORLIN RJ et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 2; PP. 391-393; BIBL. 11 REF.Article

THE DEL(4)(Q31) SYNDROME: A RECOGNIZABLE DISORDER WITH ATYPICAL ROBIN MALFORMATION SEQUENCEDAVIS JM; CLARREN SK; SALK DJ et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 2; PP. 113-117; BIBL. 11 REF.Article

Chromosome 4q deletion syndrome: a case reportBERGER, A; DAR, H; REITER, A et al.Israel journal of medical sciences. 1983, Vol 19, Num 9, pp 850-852, issn 0021-2180Article

TWO CHILDREN WITH DELETION OF THE LONG ARM OF CHROMOSOME 4 WITH BREAKPOINT AT BAND Q33TOMKINS DJ; HUNTER AGW; UCHIDA IA et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 6; PP. 348-355; BIBL. 14 REF.Article

Tentative assignment of piebald trait gene to chromosome band 4q12HOO, J. J; HASLAM, R. H. A; VAN ORMAN, C et al.Human genetics. 1986, Vol 73, Num 3, pp 230-231, issn 0340-6717Article

Four cases of partial trisomy 4p by preferential segregation in a familial 4p/17q balanced translocationDEL MAZO, J; FLORIT, F; CALAFELL, R et al.Human genetics. 1984, Vol 66, Num 4, issn 0340-6717, 370Article

Toward the complete genomic map and molecular pathology of human chromosome 4RIESS, O; WINKELMANN, B; EPPLEN, J. T et al.Human genetics. 1994, Vol 94, Num 1, pp 1-18, issn 0340-6717Article

International workshop on human chromosome 4 mappingMYERS, R. M; VAN OMMEN, G.-J.Cytogenetics and cell genetics. 1994, Vol 66, Num 4, pp 217-236, issn 0301-0171Conference Proceedings

Assignment of the human carboxypeptidase E (CPE) gene to chromosome 4HALL, C; MANSER, E; SPURR, N. K et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 2, pp 461-463, issn 0888-7543Article

Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1MORRISON, N; HARRAP, S. B; ARRIZA, J. L et al.Human genetics. 1990, Vol 85, Num 1, pp 130-132, issn 0340-6717, 3 p.Article

Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4 [HGM provisional no. D4S139]MILNER, E. C. B; LOTSHAW, C. L; VAN DIJK, K. W et al.Nucleic acids research. 1989, Vol 17, Num 10, issn 0305-1048, 4002Article

Chromosomal assignment of 20 cDNAs using flow-sorted spot-blot stampsGHISO, N. S; EVELETH, G. G; LIEUALLEN, K et al.Genomics (San Diego, Calif.). 1995, Vol 28, Num 3, pp 570-572, issn 0888-7543Article

Dinucleotide repeat polymorphisms at the D4S126 and D4S114 lociTAGLE, D. A; BLANCHARD-MCQUATE, K. L; VALDES, J et al.Human molecular genetics (Print). 1993, Vol 2, Num 7, issn 0964-6906, p. 1077Article

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