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Results: 1-12 |
Results: 12
Sequence-based design of single-copy genomic DNA probes for fluorescence in situ hybridization
Authors: Rogan, PK Cazcarro, PM Knoll, JHM
Citation: Pk. Rogan et al., Sequence-based design of single-copy genomic DNA probes for fluorescence in situ hybridization, GENOME RES, 11(6), 2001, pp. 1086-1094
Splice-site mutations and atherosclerosis: mechanisms and prediction models
Authors: von Kodolitsch, Y Nienaber, CA Fliegner, M Rogan, PK
Citation: Y. Von Kodolitsch et al., Splice-site mutations and atherosclerosis: mechanisms and prediction models, Z KARDIOL, 90(2), 2001, pp. 87
Redundant designations of BRCA1 intron 11 splicing mutation; c. 4216-2A > G; IVS11-2A > G; L78833, 37698, A > G
Authors: Svojanovsky, SR Schneider, TD Rogan, PK
Citation: Sr. Svojanovsky et al., Redundant designations of BRCA1 intron 11 splicing mutation; c. 4216-2A > G; IVS11-2A > G; L78833, 37698, A > G, HUM MUTAT, 16(3), 2000, pp. 264-264
Mosaicism in Prader-Willi syndrome - Reply
Authors: Mowery-Rushton, PA Hanchett, JM Zipf, WB Rogan, PK Surti, U
Citation: Pa. Mowery-rushton et al., Mosaicism in Prader-Willi syndrome - Reply, AM J MED G, 90(2), 2000, pp. 177-177
Exon skipping in IVD RNA processing in isovaleric acidemia caused by pointmutations in the coding region of the IVD gene
Authors: Vockley, J Rogan, PK Anderson, BD Willard, J Seelan, RS Smith, DI Liu, WG
Citation: J. Vockley et al., Exon skipping in IVD RNA processing in isovaleric acidemia caused by pointmutations in the coding region of the IVD gene, AM J HU GEN, 66(2), 2000, pp. 356-367
Information analysis of human splice site mutations. (vol 12, pg 153, 1998)
Authors: Rogan, PK Faux, BM Schneider, TD
Citation: Pk. Rogan et al., Information analysis of human splice site mutations. (vol 12, pg 153, 1998), HUM MUTAT, 13(1), 1999, pp. 82-82
Maternal uniparental disomy of chromosome 21 in a normal child
Authors: Rogan, PK Sabol, DW Punnett, HH
Citation: Pk. Rogan et al., Maternal uniparental disomy of chromosome 21 in a normal child, AM J MED G, 83(1), 1999, pp. 69-71
Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2)
Authors: Martin, RA Sabol, DW Rogan, PK
Citation: Ra. Martin et al., Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2), J MED GENET, 36(8), 1999, pp. 633-636
Splice-site mutations in atherosclerosis candidate genes - Relating individual information to phenotype
Authors: von Kodolitsch, Y Pyeritz, RE Rogan, PK
Citation: Y. Von Kodolitsch et al., Splice-site mutations in atherosclerosis candidate genes - Relating individual information to phenotype, CIRCULATION, 100(7), 1999, pp. 693-699
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints
Authors: Amos-Landgraf, JM Ji, YG Gottlieb, W Depinet, T Wandstrat, AE Cassidy, SB Driscoll, DJ Rogan, PK Schwartz, S Nicholls, RD
Citation: Jm. Amos-landgraf et al., Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints, AM J HU GEN, 65(2), 1999, pp. 370-386
Imprinting-mutation mechanisms in Prader-Willi syndrome
Authors: Ohta, T Gray, TA Rogan, PK Buiting, K Gabriel, JM Saitoh, S Muralidhar, B Bilienska, B Krajewska-Walasek, M Driscoll, DJ Horsthemke, B Butler, MG Nicholls, RD
Citation: T. Ohta et al., Imprinting-mutation mechanisms in Prader-Willi syndrome, AM J HU GEN, 64(2), 1999, pp. 397-413
Relaxation of imprinting in Prader-Willi syndrome
Authors: Rogan, PK Seip, JR White, LM Wenger, SL Steele, MW Sperling, MA Menon, R Knoll, JHM
Citation: Pk. Rogan et al., Relaxation of imprinting in Prader-Willi syndrome, HUM GENET, 103(6), 1998, pp. 694-701
Risultati: 1-12 |