Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Chromosome D13")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 975

  • Page / 39
Export

Selection :

  • and

The DNA sequence and analysis of human chromosome 13DUNHAM, A; MATTHEWS, L. H; JONES, M. C et al.Nature (London). 2004, Vol 428, Num 6982, pp 522-528, issn 0028-0836, 7 p.Article

RING CHROMOSOME 13 IN A POLYMALFORMED ANENCEPHALIC = CHROMOSOME 13 EN ANNEAU CHEZ UN ANENCEPHALE POLYMALFORMESCHMID W; MUEHLETHALER JP; BRINER J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 1; PP. 63-66; BIBL. 6REF.Article

CHROMOSOME 13 EN ANNEAUHEVIA A; BULLON M; NOVALES A et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 232-233; ABS. ENG; BIBL. 7 REF.Article

HUMAN ACROCENTRIC RING CHROMOSOMES AND SATELLITE ASSOCIATION.CANTU JM; SALAMANCA F; SANCHEZ J et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 3; PP. 193-196; ABS. FR.; BIBL. 23 REF.Article

A CASE OF D13 RING CHROMOSOMECOSSU P; DIANA G; MAMELI M et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 111-114; BIBL. 10 REF.Article

Localization of the human homologue of the Drosophila dachshund gene (DACH) to chromosome 13q21KOZMIK, Z; CVEKL, A.Genomics (San Diego, Calif.). 1999, Vol 59, Num 1, pp 110-111, issn 0888-7543Article

Assignment of the human GAS6 gene to chromosome 13q34 by fluorescence in situ hybridizationSACCONE, S; MARCANDALLI, P; GOSTISSA, M et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 1, pp 129-131, issn 0888-7543Article

RING CHROMOSOME 13 IN A CHILD WITH MINOR DYSMORPHIC FEATURES, IRREGULAR PHENOTYPIC EXPRESSION OF RING 13 SYNDROMEVERMA RS; DOSIK H; CHOWDHRY IH et al.1978; AMER. J. DIS. CHILD; USA; DA. 1978; VOL. 132; NO 10; PP. 1018-1021; BIBL. 21 REF.Article

IRREGULAR PHENOTYPIC EXPRESSION OF RING CHROMOSOMES = EXPRESSION PHENOTYPIQUE IRREGULIERE DES CHROMOSOMES ANNULAIRESZDANSKY R; ANDRLE M; BUEHLER E et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 3; PP. 193-198; ABS. ALLEM.; BIBL. 14REF.Article

PARENTAL ORIGIN OF A RING 13 CHROMOSOME IN A FEMALE WITH MULTIPLE ANOMALIES.MAGENIS RE; WYANDT HE; OVERTON KM et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 181-186; BIBL. 9 REF.Article

Interstitial deletion of long arm of chromosome 13CARNEVALE, A; FRIAS, S; ALCANTAR, R et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 49-52, issn 0003-3995Article

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21BLOUIN, J.-L; DOMBROSKI, B. A; LAMACZ, M et al.Nature genetics. 1998, Vol 20, Num 1, pp 70-73, issn 1061-4036Article

Fine structure physical mapping of a 1.9 Mb region of chromosome 13q12STILL, I. H; ROBERTS, T; COWELL, J. K et al.Annals of human genetics. 1997, Vol 61, pp 15-24, issn 0003-4800, 1Article

The human FGF9 gene maps to chromosomal region 13q11-q12MATTEI, M.-G; PENAULT-LLORCA, F; COULIER, F et al.Genomics (San Diego, Calif.). 1995, Vol 29, Num 3, pp 811-812, issn 0888-7543Article

High-resolution YAC-cosmid-STS map of human chromosome 13CAYANIS, E; RUSSO, J. J; BENTO SOARES, M et al.Genomics (San Diego, Calif.). 1998, Vol 47, Num 1, pp 26-43, issn 0888-7543Article

Trisomy 13/trisomy 18 mosaicism in an infantABE, K; HARADA, N; ITOH, T et al.Clinical genetics. 1996, Vol 50, Num 5, pp 300-303, issn 0009-9163Article

UNUSUAL 13/13 TRANSLOCATION AND 13 TRISOMY PHENOTYPEFRYNS JP; KLECZKOWSKA A; KUBIEN E et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 113-115; ABS. FRE; BIBL. 5 REF.Article

LONG SURVIVAL IN TRISOMY-13-SYNDROME: 21 CASES INCLUDING PROLONGED SURVIVAL IN TWO PATIENTS 11 AND 19 YERS OLDREDHEENDRAN R; NEU RL; BANNERMAN RM et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 2; PP. 167-172; BIBL. 7 REF.Article

Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11→q12 and mouse chromosome 14D1-E1 by in situ hybridizationMIGNON, C; FROMAGET, C; MATTEI, M.-G et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 2-3, pp 185-186, issn 0301-0171Conference Paper

Clinical delineation of proximal and distal partial 13q trisomyROGERS, J. F.Clinical genetics. 1984, Vol 25, Num 3, pp 221-229, issn 0009-9163Article

PERICENTRIC INVERSION OF CHROMOSOME NO. 13 IN A LARGE FAMILY LEADING TO DUPLICATION DEFICIENCY CAUSING CONGENITAL MALFORMATIONS IN THREE INDIVIDUALS = INVERSION PERICENTRIQUE DU CHROMOSOME NO13 DANS UNE IMPORTANTE FAMILLE CONDUISANT A UNE DUPLICATION AVEC DEFICIT CAUSE DE MALFORMATIONS CONGENITALES CHEZ TROIS INDIVIDUSHAUKSDOTTIR H; HALLDORSSON S; JENSSON O et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 413-421; BIBL. 10REF.Serial Issue

Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomyBEREND, S. A; FELDMAN, G. L; MCCASKILL, C et al.American journal of medical genetics. 1999, Vol 82, Num 3, pp 275-281, issn 0148-7299Article

A DOUBLE ANEUPLOID MOSAIC: TRISOMY 13 AND XXY = MOSAIQUE ANEUPLOIDE DOUBLE AVEC TRISOMIE 13 ET XXYEBBIN AJ; CHU LIM R; TOWNER JW et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 365-367; BIBL. 1 REF.Serial Issue

D1 RING CHROMOSOME IN NEWBORN WITH PECULIAR FACE, POLYDACTYLY, IMPERFORATE ANUS, ARRHINENCEPHALY, AND OTHER MALFORMATIONS = CHROMOSOME D1 EN ANNEAU CHEZ UN NOUVEAU-NE AVEC FACIES PARTICULIER, POLYDACTYLIE, IMPERFORATION ANALE, ARRHINENCEPHALIE ET D'AUTRES MALFORMATIONSBILES AR JR; LUEERS T; SPERLING K et al.1970; J. MED. GENET.; G.B.; DA. 1970; VOL. 7; NO 4; PP. 399-401; BIBL. 17 REF.Serial Issue

Trisomy 13 appearing as a mimic of a triploid partial moleCURTIN, William M; MARCOTTE, Michael P; MYERS, Linda L et al.Journal of ultrasound in medicine. 2001, Vol 20, Num 10, pp 1137-1139, issn 0278-4297Article

  • Page / 39