RING CHROMOSOME 17 IN A MENTALLY RETARTED YOUNG MAN: CLINICAL, CYTOGENETIC AND BIOCHEMICAL INVESTIGATIONSCHUDLEY AE; PABELLO PD; MCALPINE PJ et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 12; NO 2; PP. 219-225; BIBL. 16 REF.Article

A centromere-based linkage group on the long arm of human chromosome 17TSIPOURAS, P; SCHWARTZ, R. C; PHILLIPS, J. A. III et al.Cytogenetics and cell genetics. 1988, Vol 47, Num 1-2, pp 109-110, issn 0301-0171Article

CHROMOSOME 17 HAS A REAL FRAGILE SITE AT P12SHABTAI F; KLAR D; HALBRECHT I et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 2; PP. 177-179; BIBL. 6 REF.Article

HUMAN TYPE I PROCOLLAGEN GENES ARE LOCATED ON DIFFERENT CHROMOSOMESHUERRE C; JUNIEN C; WEIL D et al.1982; PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. BIOLOGICAL SCIENCES; ISSN 0273-1134; USA; DA. 1982; VOL. 79; NO 21; PP. 6627-6630; BIBL. 39 REF.Article

CLINICAL SIGNIFICANCE OF THE SATELLITED SHORT ARM OF HUMAN CHROMOSOME 17 (17PS+): A RARE HETEROMORPHISMVERMA RS; BRAT SV; WARMAN J et al.1979; AM. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 133-136; ABS. FRE; BIBL. 20 REF.Article

The gene cluster for human U2 RNA is located on chromosome 17q21HAMMARSTROM, K; SANTESSON, B; WESTIN, G et al.Experimental cell research. 1985, Vol 159, Num 2, pp 473-478, issn 0014-4827Article

A moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11-17q22)MURPHY, P. D; FERGUSON-SMITH, A. C; MIKI, T et al.Nucleic acids research. 1987, Vol 15, Num 15, issn 0305-1048, 6311Article

Homozygosity for fragile site at 17p12 in a 28-year-old healthy manIZAKOVIC, V.Human genetics. 1984, Vol 68, Num 4, pp 340-341, issn 0340-6717Article

Assignment of human platelet GP2B (GPIIb) gene to chomosome 17, region q21.1-q21.3NGUYEN VAN CONG; UZAN, G; GROSS, M. S et al.Human genetics. 1988, Vol 80, Num 4, pp 389-392, issn 0340-6717Article

Human p53 gene localized to short arm of chromosome 17MILLER, C; MOHANDAS, T; WOLF, D et al.Nature (London). 1986, Vol 319, Num 6056, pp 783-784, issn 0028-0836Article

Translocation (15;17) in a child with variant form of acute promyelocytic leukemia = Translocation (15; 17) chez un enfant présentant une variante de leucémie aiguë promyélocytairePRIETO, F; BADIA, L; CASTEL, V et al.Cancer genetics and cytogenetics. 1983, Vol 10, Num 1, pp 117-120, issn 0165-4608Article

LA TRISOMIE 17PRETHORE MO; RENAULT F; LAFOURCADE J et al.1983; SEMAINE DES HOPITAUX; ISSN 0037-1777; FRA; DA. 1983; VOL. 59; NO 27-28; PP. 2039-2042; ABS. ENG; BIBL. 8 REF.Article

SILVER STAINING STUDIES ON THE SHORT ARM VARIANT OF HUMAN CHROMOSOME 17.OLIVER N; FRANCKE U; TAYLOR KM et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 42; NO 1; PP. 79-82; BIBL. 10 REF.Article

ABNORMALITIES OF CHROMOSOME NO 17 IN MYELOPROLIFERATIVE DISORDERSBORGSTROEM GH; VUOPLO P; DE LA CHAPELLE A et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 5; NO 2; PP. 123-135; BIBL. 26 REF.Article

SIGNIFICANCE OF 17 VARIANT CHROMOSOME IN THREE FAMILIESMARCUCCI L; PETRINELLI P; ANTONELLI A et al.1980; CARYOLOGIA; ISSN 0008-7114; ITA; DA. 1980; VOL. 33; NO 1; PP. 117-122; BIBL. 15 REF.Article

INTERPRETATION OF A MARKER CHROMOSOME 17P IN MULTIPLE MYELOMASHABTAI F; HALBRECHT I.1981; HEREDITAS; ISSN 0018-0661; SWE; DA. 1981; VOL. 95; NO 1; PP. 11-14; BIBL. 14 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

The human cytochrome b561 gene (CYB561) is located at 17q11-qterMCBRIDE, O. W; HUA FANG YI; SRIVASTAVA, M et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 3, pp 662-663, issn 0888-7543Article

Localization of glucose-dependent insulinotropic polypeptide (GIP) to a gene cluster on chromosome 17qLEWIS, T. B; SAENZ, M; O'CONNELL, P et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 3, pp 589-591, issn 0888-7543Article

CRK proto-oncogene maps to human chromosome band 17p13FIORETOS, J; HEISTERKAMP, N; GROFFEN, J et al.Oncogene (Basingstoke). 1993, Vol 8, Num 10, pp 2853-2855, issn 0950-9232Article

The case of the gray optic disc!BRODSKY, M. C; BUCKLEY, E. G; MCCONKIE-ROSELL, A et al.Survey of ophthalmology. 1989, Vol 33, Num 5, pp 367-372, issn 0039-6257Article

Random cloning of genes from mouse chromosome 17KASAHARA, M; FIGUEROA, F; KLEIN, J et al.Proceedings of the National Academy of Sciences of the United States of America. 1987, Vol 84, Num 10, pp 3325-3328, issn 0027-8424Article

Physical mapping of chromosome 17 cosmids by fluorescence in sity hybridization and digital image analysisKALLIONIEMI, O.-P; KALLIONIEMI, A; MASCIO, L et al.Genomics (San Diego, Calif.). 1994, Vol 20, Num 1, pp 125-128, issn 0888-7543Article

Assignement of apolipoprotein H (APOH: beta-2-glycoprotein I) to human chromosome 17q23→qter; determination of the major expression siteSTEINKASSERER, A; COCKBURN, D. J; BLACK, D. M et al.Cytogenetics and cell genetics. 1992, Vol 60, Num 1, pp 31-33, issn 0301-0171Article

A CA dinucleotide polymorphism at D17S107 (17q12-q24)BARKER, D. F; NGUYEN, K; FAIN, P. R et al.Human molecular genetics (Print). 1993, Vol 2, Num 7, issn 0964-6906, p. 1086Article