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Results: 1-15 |
Results: 15
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel
Authors: Tuck-Muller, CM Goodman, BK Li, SB Martinez, JE Chen, XN Wertelecki, W Korenberg, JR Stetten, G
Citation: Cm. Tuck-muller et al., Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel, GENET MED, 3(2), 2001, pp. 126-131
Non-mosaic trisomy 20 presenting at 21 weeks' gestation as a thoraco-abdominal mass
Authors: Driggers, RW Bernstein, H Lantz, H Stetten, G Escallon, CS Perlman, E Blakemore, KJ
Citation: Rw. Driggers et al., Non-mosaic trisomy 20 presenting at 21 weeks' gestation as a thoraco-abdominal mass, PRENAT DIAG, 21(5), 2001, pp. 387-389
A Cre-lox recombination system for the targeted integration of circular yeast artificial chromosomes into embryonic stem cells
Authors: Call, LM Moore, CS Stetten, G Gearhart, JD
Citation: Lm. Call et al., A Cre-lox recombination system for the targeted integration of circular yeast artificial chromosomes into embryonic stem cells, HUM MOL GEN, 9(12), 2000, pp. 1745-1751
Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome
Authors: Norris, RA Scott, KK Moore, CS Stetten, G Brown, CR Jabs, EW Wulfsberg, EA Yu, J Kern, MJ
Citation: Ra. Norris et al., Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome, MAMM GENOME, 11(11), 2000, pp. 1000-1005
Real-time volumetric echocardiography: The technology and the possibilities
Authors: Kisslo, J Firek, B Ota, T Kang, DH Fleishman, CE Stetten, G Li, J Ohazama, CJ Adams, D Landolfo, C Ryan, T von Ramm, O
Citation: J. Kisslo et al., Real-time volumetric echocardiography: The technology and the possibilities, ECHOCARDIOG, 17(8), 2000, pp. 773-779
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13,18, 20 and 21: karyotype-phenotype correlations
Authors: Wallerstein, R Yu, MT Neu, RL Benn, P Bowen, CL Crandall, B Disteche, C Donahue, R Harrison, B Hershey, D Higgins, RR Jenkins, LS Jackson-Cook, C Keitges, E Khodr, G Lin, CC Luthardt, FW Meisner, L Mengden, G Patil, SR Rodriguez, M Sciorra, LJ Shaffer, LG Stetten, G Van Dyke, DL Wang, HS Williams, F Zaslav, AL Hsu, LYF
Citation: R. Wallerstein et al., Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13,18, 20 and 21: karyotype-phenotype correlations, PRENAT DIAG, 20(2), 2000, pp. 103-122
Assessment of regional wall motion abnormalities with real-time 3-dimensional echocardiography
Authors: Collins, M Hsieh, A Ohazama, CJ Ota, T Stetten, G Donovan, CL Kisslo, J Ryan, T
Citation: M. Collins et al., Assessment of regional wall motion abnormalities with real-time 3-dimensional echocardiography, J AM S ECHO, 12(1), 1999, pp. 7-14
Integration of cytogenetic with recombinational and physical maps of mousechromosome 16
Authors: Moore, CS Lee, JS Birren, B Stetten, G Baxter, LL Reeves, RH
Citation: Cs. Moore et al., Integration of cytogenetic with recombinational and physical maps of mousechromosome 16, GENOMICS, 59(1), 1999, pp. 1-5
Revised genomic organization of FBN1 and significance for regulated gene expression
Authors: Biery, NJ Eldadah, ZA Moore, CS Stetten, G Spencer, F Dietz, HC
Citation: Nj. Biery et al., Revised genomic organization of FBN1 and significance for regulated gene expression, GENOMICS, 56(1), 1999, pp. 70-77
X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes
Authors: Smith, KD Kemp, S Braiterman, LT Lu, JF Wei, HM Geraghty, M Stetten, G Bergin, JS Pevsner, J Watkins, PA
Citation: Kd. Smith et al., X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes, NEUROCHEM R, 24(4), 1999, pp. 521-535
Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat
Authors: Goodman, BK Stone, K Coddett, JM Cargile, CB Gurewitsch, ED Blakemore, KJ Stetten, G
Citation: Bk. Goodman et al., Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat, PRENAT DIAG, 19(12), 1999, pp. 1150-1156
Turkey - From hatchling to the store counter
Authors: Stetten, G
Citation: G. Stetten, Turkey - From hatchling to the store counter, FLEISCHWIRT, 79(1), 1999, pp. 36-36
Real-time, three-dimensional echocardiography: Feasibility of dynamic right ventricular volume measurement with saline contrast
Authors: Ota, T Fleishman, CE Strub, M Stetten, G Ohazama, CJ von Ramm, OT Kisslo, J
Citation: T. Ota et al., Real-time, three-dimensional echocardiography: Feasibility of dynamic right ventricular volume measurement with saline contrast, AM HEART J, 137(5), 1999, pp. 958-966
Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene
Authors: Bjorkman, J Stetten, G Moore, CS Gould, SJ Crane, DI
Citation: J. Bjorkman et al., Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene, GENOMICS, 54(3), 1998, pp. 521-528
Isolation and characterization of the human gene encoding I-to: further diversity by alternative mRNA splicing
Authors: Kong, W Po, S Yamagishi, T Ashen, MD Stetten, G Tomaselli, GF
Citation: W. Kong et al., Isolation and characterization of the human gene encoding I-to: further diversity by alternative mRNA splicing, AM J P-HEAR, 44(6), 1998, pp. H1963-H1970
Risultati: 1-15 |