Zobrazeno 1 - 10
of 289
pro vyhledávání: '"Roger A. Schultz"'
Autor:
Montelone, Beth A
Publikováno v:
The Quarterly Review of Biology, 2006 Sep . 81(3), 273-273.
Externí odkaz:
https://www.jstor.org/stable/10.1086/509407
Autor:
Roger E. Schultz, Michal Tavrovsky
Publikováno v:
Journal of Urology. 206
INTRODUCTION AND OBJECTIVE:We compared standard Prometheus Office Uroflowmetry (POU) against the results obtained by a new MenHealth Uroflowmetry App (MUA). The MenHealth Uroflowmetry App (MUA) is ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dd38fab16027a1d3f3a68536f61040a
https://doi.org/10.1097/ju.0000000000001963.10
https://doi.org/10.1097/ju.0000000000001963.10
Autor:
Denise I. Quigley, Timothy Tidwell, Brandon Chandler, Erica F. Andersen, Roger A. Schultz, Zoe K Lewis, Allen N. Lamb, Patricia Mowery-Rushton, Xinjie Xu, Adam L. Clayton, Reha M. Toydemir, Julie L Cox, Bo Hong
Publikováno v:
Cancer Genetics. :S15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e8125191476b1c71a3f5a4029463531
https://doi.org/10.1016/j.cancergen.2021.01.055
https://doi.org/10.1016/j.cancergen.2021.01.055
Autor:
Megan E. Tucker, Luis F. Escobar, David Chitayat, Nicholas J. Neill, Beth S. Torchia, Roger A. Schultz, Karen Chong, Jill A. Rosenfeld, Lisa D McDaniel
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 46:478-486
Objectives To determine the frequency of clinically significant chromosomal abnormalities identified by chromosomal microarray in pregnancy losses at any gestational age and to compare microarray performance with that of traditional cytogenetic analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c022642517469c78c4b8fac170e4c3d0
https://doi.org/10.1002/uog.14866
https://doi.org/10.1002/uog.14866
Publikováno v:
National Guard. Aug98, Vol. 52 Issue 8, p16. 3p. 1 Color Photograph.
Autor:
Justin Overhoff, Jill A. Rosenfeld, Jay W. Ellison, Lynne M. Bird, Roger A. Schultz, Karla Haynes, Lisa G. Shaffer, Marina Rabideau, Daniela N. Schweitzer
Publikováno v:
American Journal of Medical Genetics Part A. 164:259-263
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c147e41edf566d836dd7a104fd3a5c9c
https://doi.org/10.1002/ajmg.a.36163
https://doi.org/10.1002/ajmg.a.36163
Autor:
Mark Fesler, Roger A. Schultz, Jacqueline R. Batanian, Raymond R. Tubbs, Blake C. Ballif, Heesun J. Rogers, Aaron M. Gruver, James R. Cook
Publikováno v:
Diagnostic Molecular Pathology. 22:10-21
Acute promyelocytic leukemia (APL) is typically defined at the molecular level by a reciprocal translocation of the promyelocytic leukemia (PML) and retinoic acid receptor α (RARA) genes. An accurate diagnosis of APL is critical for appropriate choi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e86edf03ad77a11b2a0140a66cb40b7
https://doi.org/10.1097/pdm.0b013e31825b8326
https://doi.org/10.1097/pdm.0b013e31825b8326
Autor:
Hans Lehrach, Roger A. Schultz, Zdenek Trachtulec, Elsy P. Jones, Hong Xiao, Kirsten Fischer Lindahl, Zoia Larin, Lorraine Flaherty, Vladimir Vincek
Sixteen yeast artificial chromosome (YAC) clones have been mapped to the H2-M region at the distal end of the mouse major histocompatibility complex (MHC) on chromosome 17. Analysis of the YACs with single and multicopy probes yielded a proximal cont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d711bead226e1e2fc4f0f5bdd68c8e6c
https://doi.org/10.1006/geno.1995.1006
https://doi.org/10.1006/geno.1995.1006
Autor:
Michael E. Talkowski, Blake C. Ballif, Roger A. Schultz, Patricia I. Bader, Susan Sell, Zheng Fan, James F. Gusella, Debra J Keelean-Fuller, Suneeta Madan-Khetarpal, Loren Mackay-Loder, Deborah Terespolsky, Urvashi Surti, Jill Pouncey, Santhosh Girirajan, Marilyn C. Jones, Bénédicte Héron‐Longe, Ian Blumenthal, Kenneth N. Rosenbaum, Maria Descartes, Jill A. Rosenfeld, Cynthia C. Morton, Evan E. Eichler, Gwen M. Glew, Alain Verloes, Amy Shealy, Sandrine Passemard, Brigitte Benzacken, Cathy A. Stevens, Eva Pipiras, Nicholas J. Neill, Roger L. Ladda, Rocio Moran, Lisa G. Shaffer, John B. Moeschler, Allen N. Lamb, Judith A. Martin, Stephanie E. Vallee, Kent E. Opheim, Juliann Mcconnell, Bertrand Isidor, Andrée Delahaye, Cédric Le Caignec, Shawnia Ryan
Publikováno v:
Human Mutation. 33:728-740
SOX5 encodes a transcription factor involved in the regulation of chondrogenesis and the development of the nervous system. Despite its important developmental roles, SOX5 disruption has yet to be associated with human disease. We report one individu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04d6ce34aa6fb60ead0a602f177b7a93
https://doi.org/10.1002/humu.22037
https://doi.org/10.1002/humu.22037
Autor:
T.A. Smolarek, Jerome L. Gorski, Y. Senturias, M. Frydman, Blake C. Ballif, Jill A. Rosenfeld, Jay W. Ellison, D. Earl, Robin Troxell, B. Torchia, Karen D. Tsuchiya, Roger A. Schultz, M. Westemeyer, Brad Angle, Lisa G. Shaffer, S. Zimmerman, Katherine H. Kim
Publikováno v:
Molecular Syndromology. 3:247-254
Microduplications of the Sotos syndrome region containing NSD1 on 5q35 have recently been proposed to cause a syndrome of microcephaly, short stature and developmental delay. To further characterize this emerging syndrome, we report the clinical deta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::811e63bd233216b286120529a1f9cbad
https://doi.org/10.1159/000345578
https://doi.org/10.1159/000345578