Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Chromosome 15")

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 248

  • Page / 10
Export

Selection :

  • and

NONRANDOM ASSOCIATION BETWEEN A SPECIFIC AUTOSOME AND THE X CHROMOSOME IN MEIOSIS OF THE MALE MOUSE: POSSIBLE CONSEQUENCE OF THE HOMOLOGUES CENTROMERES' SEPARATION = ASSOCIATION NON ALEATOIRE ENTRE UN AUTOSOME SPECIFIQUE ET LE CHROMOSOME X A LA MEIOSE DE LA SOURIS MALE. CONSEQUENCE POSSIBLE DE LA SEPARATION DES CENTROMERES HOMOLOGUESFOREJT J.1974; CYTOGENET. CELL GENET.; SWITZ.; DA. 1974; VOL. 13; NO 4; PP. 369-383; BIBL. 2 P. 1/2Article

Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic herniaHATEM, Elghezal; BEN REKAYA MERIAM; WALID, Denguezli et al.Prenatal diagnosis. 2007, Vol 27, Num 5, pp 471-474, issn 0197-3851, 4 p.Article

Possible Genetic Heterogeneity of Spinocerebellar Ataxia Linked to Chromosome 15WEISSBACH, Anne; DJARMATI, Ana; PETROVIC, Igor et al.Movement disorders. 2010, Vol 25, Num 11, pp 1577-1582, issn 0885-3185, 6 p.Article

Detection of an unexpected subtelomeric 15q26.2→qter deletion in a little girl : Clinical and cytogenetic studiesPINSON, L; PERRIN, A; PLOUZENNEC, C et al.American journal of medical genetics. 2005, Vol 138A, Num 2, pp 160-165, issn 0148-7299, 6 p.Article

15q11.2 Proximal Imbalances Associated With a Diverse Array of Neuropsychiatric Disorders and Mild Dysmorphic FeaturesABDELMOITY, Ahmed T; LEPICHON, Jean-Baptiste; NYP, Sarah S et al.Journal of developmental and behavioral pediatrics. 2012, Vol 33, Num 7, pp 570-576, issn 0196-206X, 7 p.Article

Genetics of childhood disorders: XLVII. Autism, Part 6: Duplication and inherited susceptibility of chromosome 15q11-q13 genes in autismSUTCLIFFE, James S; NURMI, Erika L.Journal of the American Academy of Child and Adolescent Psychiatry. 2003, Vol 42, Num 2, pp 253-256, issn 0890-8567, 4 p.Article

Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15JOVANOVIE-PRIVRODSKI, Jadranka D; KAVECAN, Ivana I; OBRENOVIC, Milan R et al.Pediatric neurology. 2009, Vol 41, Num 1, pp 65-67, issn 0887-8994, 3 p.Article

Generation and characterization of a 12,000-rad radiation hybrid panel for fine mapping in pigYERLE, M; PINTON, P; DELCROS, C et al.Cytogenetic and genome research. 2002, Vol 97, Num 3-4, pp 219-228, issn 1424-8581, 10 p.Article

Chromosome 15 aneuploidy in the sperm and conceptus of a sibling with variable familial expression of round-headed sperm syndromeCARRELL, Douglas T; WILCOX, Aaron L; UDOFF, Laurence C et al.Fertility and sterility. 2001, Vol 76, Num 6, pp 1258-1260, issn 0015-0282Article

Mapping of the titin (TTN) gene to pig chromosome 15BERTANI, G. R; LARSEN, N. J; MARKLUND, S et al.Journal of animal science. 1999, Vol 77, Num 10, pp 2857-2858, issn 0021-8812Article

Mapping of the Steroidogenic Acute Regulatory Protein (StAR) gene to porcine chromosome 15 by linkage analysis using a novel PCR-RFLPSPLAN, R. K; PILCIK, B. R; MOODY, D. E et al.Journal of animal science. 1998, Vol 76, Num 2, pp 658-659, issn 0021-8812Article

Autism in Angelman syndrome : A population-based studySTEFFENBURG, S; GILLBERG, C. L; STEFFENBURG, U et al.Pediatric neurology. 1996, Vol 14, Num 2, pp 131-136, issn 0887-8994Article

The RB gene locates on chromosome 15 at band 15q13 in the Syrian hamsterSATOH, H; EBERT, R; WISEMAN, R. W et al.Cytogenetics and cell genetics. 1994, Vol 65, Num 1-2, pp 127-129, issn 0301-0171Conference Paper

Comparative cytogenetic mapping of COL14A1, the gene for human and mouse collagen XIVIMHOF, M; TRUEB, B.Cytogenetics and cell genetics. 1999, Vol 84, Num 3-4, pp 217-219, issn 0301-0171Article

Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15L'HERMINE, A. Coulomb; ABOURA, A; BRISSET, S et al.Prenatal diagnosis. 2003, Vol 23, Num 11, pp 938-943, issn 0197-3851, 6 p.Article

RING CHROMOSOME 15: EXPANDING THE PHENOTYPEEID, M. M; EL-BASSYOUNI, H. T; EID, O. M et al.Genetic counseling. 2013, Vol 24, Num 4, pp 417-425, issn 1015-8146, 9 p.Article

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGHMANOLAKOS, Emmanouil; VETRO, Annalisa; LIEHR, Thomas et al.Prenatal diagnosis. 2009, Vol 29, Num 9, pp 884-888, issn 0197-3851, 5 p.Article

SPECIFICITY OF THE DELETION OF CHROMOSOME 15 IN MOUSE PLASMACYTOMA: BRIEF COMMUNICATION.YOSHIDA MC; MORIWAKI K; MIGITA S et al.1978; J. NATION. CANCER INST.; U.S.A.; DA. 1978; VOL. 60; NO 1; PP. 235-238; BIBL. 17 REF.Article

Human and mouse GPAA1 (Glycosylphosphatidylinositol anchor attachment 1) genes : genomic structures, chromosome loci and the presence of a minor class intronINOUE, N; OHISHI, K; ENDO, Y et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 3-4, pp 199-205, issn 0301-0171Article

Assignment of Pdnp2, the gene encoding phosphodiesterase I/nucleotide pyrophosphatase 2, to mouse Chromosome 15D2PIAO, J.-H; MATSUDA, Y; NAKAMURA, H et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 3-4, pp 172-174, issn 0301-0171Article

Genetic mapping of the mouse genes encoding the voltage-sensitive calcium channel subunitsHEMIN CHIN; OH-JOO KWON; HYUN HO JUNG et al.Genomics (San Diego, Calif.). 1995, Vol 28, Num 3, pp 592-595, issn 0888-7543Article

TaqI RFLPs at the bovine uroplakin II locus (UPK2)RYAN, A. M; WOMACK, J. E; LIN, J.-H et al.Animal genetics (Print). 1994, Vol 25, Num 1, issn 0268-9146, p. 58Article

The mouse and human excitatory amino acid transporter gene (EAAT1) maps to mouse chromosome 15 and a region of syntenic homology on human chromosome 5KIRSCHNER, M. A; ARRIZA, J. L; COPELAND, N. G et al.Genomics (San Diego, Calif.). 1994, Vol 22, Num 3, pp 631-633, issn 0888-7543Article

Molecular genetics of autism spectrum disorderVEENSTRA-VANDERWEELE, J; COOK, E. H.Molecular psychiatry. 2004, Vol 9, Num 9, pp 819-832, issn 1359-4184, 14 p.Article

Chromosomal mapping of the potassium channel genes Kcnq2 and Kcnq3 in mouseMCCORMACK, T; RUDY, B; SELDIN, M. F et al.Genomics (San Diego, Calif.). 1999, Vol 56, Num 3, pp 360-361, issn 0888-7543Article

  • Page / 10