The cardiofaciocutaneous syndrome
Roberts, A, Allanson, J, Jadico, S K, Kavamura, M I, Noonan, J, Opitz, J M, Young, T, Neri, G
Published in Journal of Medical Genetics (01.11.2006)
Published in Journal of Medical Genetics (01.11.2006)
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Journal Article
Book Review
Blood Flow Restriction Training Using the Delfi System Is Associated With a Cellular Systemic Response
Callanan, Mark C., Plummer, Hillary A., Chapman, Garrett L., Opitz, Tyler J., Rendos, Nicole K., Anz, Adam W.
Published in Arthroscopy, Sports Medicine, and Rehabilitation (01.02.2021)
Published in Arthroscopy, Sports Medicine, and Rehabilitation (01.02.2021)
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Journal Article
Association Between Passive Hip Range of Motion and Pitching Kinematics in High School Baseball Pitchers
Plummer, Hillary A, Bordelon, Nicole M, Wasserberger, Kyle W, Opitz, Tyler J, Anz, Adam W, Oliver, Gretchen D
Published in International journal of sports physical therapy (01.01.2021)
Published in International journal of sports physical therapy (01.01.2021)
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Journal Article
A de novo splice site mutation in CASK causes FG syndrome‐4 and congenital nystagmus
Dunn, P., Prigatano, G. P., Szelinger, S., Roth, J., Siniard, A. L., Claasen, A. M., Richholt, R. F., De Both, M., Corneveaux, J. J., Moskowitz, A. M., Balak, C., Piras, I. S., Russell, M., Courtright, A. L., Belnap, N., Rangasamy, S., Ramsey, K., Opitz, J. M., Craig, D. W., Narayanan, V., Huentelman, M. J., Schrauwen, I.
Published in American journal of medical genetics. Part A (01.03.2017)
Published in American journal of medical genetics. Part A (01.03.2017)
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Journal Article
Reconstructing the evolutionary history of the artiodactyl ribonuclease superfamily
Jermann, Thomas M, Opitz, Jochen G, Stackhouse, Joseph, Benner, Steven A
Published in Nature (London) (02.03.1995)
Published in Nature (London) (02.03.1995)
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Journal Article
Assessment of an online calculator’s vancomycin dosing and exposure appropriateness in persons who inject drugs with methicillin‐resistant Staphylococcus aureus bloodstream infections
Opitz, Brandon J., Housman, Seth T., Housman, Erica L., Lorenzo, Michael P.
Published in Journal of clinical pharmacy and therapeutics (01.06.2022)
Published in Journal of clinical pharmacy and therapeutics (01.06.2022)
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Journal Article
PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome
KAVAMURA, M. I, POMPONI, M. G, ZOLLINO, M, LECCE, R, MURDOLO, M, BRUNONI, D, ALCHORNE, M. M. A, OPITZ, J. M, NERI, G
Published in European journal of human genetics : EJHG (01.01.2003)
Published in European journal of human genetics : EJHG (01.01.2003)
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Journal Article
Outcomes After Ulnar Collateral Ligament Revision Reconstruction in Baseball Players
Andrews, James R, Venkateswaran, Vikram, Christensen, Kevin D, Plummer, Hillary A, Hart, Karen M, Opitz, Tyler J, Wilk, Kevin E, Pinegar, Caleb O, Cain, Jr, E Lyle, Dugas, Jeffrey R, Jordan, Steve E, Fleisig, Glenn S
Published in The American journal of sports medicine (01.11.2020)
Published in The American journal of sports medicine (01.11.2020)
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Journal Article
Photolabile Carboxylic Acid Protected Terpolymers for Surface Patterning. Part 2: Photocleavage and Film Patterning
Millaruelo, M, Eng, L. M, Mertig, M, Pilch, B, Oertel, U, Opitz, J, Sieczkowska, B, Simon, F, Voit, B
Published in Langmuir (24.10.2006)
Published in Langmuir (24.10.2006)
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Journal Article
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
Quaderi, N A, Schweiger, S, Gaudenz, K, Franco, B, Rugarli, E I, Berger, W, Feldman, G J, Volta, M, Andolfi, G, Gilgenkrantz, S, Marion, R W, Hennekam, R C, Opitz, J M, Muenke, M, Ropers, H H, Ballabio, A
Published in Nature genetics (01.11.1997)
Published in Nature genetics (01.11.1997)
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Journal Article
Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain
Gaudenz, Karin, Roessler, Erich, Quaderi, Nandita, Franco, Brunella, Feldman, George, Gasser, David L., Wittwer, Bärbel, Montini, Eugenio, Opitz, John M., Ballabio, Andrea, Muenke, Maximilian
Published in American journal of human genetics (01.09.1998)
Published in American journal of human genetics (01.09.1998)
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Journal Article
Transitory hypogammaglobulinemia of infancy in FG syndrome
Finocchi, A., Palma, P., Rossi, P., Opitz, J.M., Neri, G.
Published in American journal of medical genetics. Part A (01.11.2005)
Published in American journal of medical genetics. Part A (01.11.2005)
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Journal Article
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
Robin, Nathaniel H, Feldman, George J, Aronson, Adam L, Mitchell, Heather F, Weksberg, Rosanna, Leonard, Claire O, Burton, Barbara K, Josephson, Kevin D, Laxová, Renata, Aleck, Kyrieckos A, Allanson, Judith E, Guion-Almeida, Maria Leine, Martin, Rick A, Leichtman, Lawrence G, Price, R. Arlen, Opitz, John M, Muenke, Maximilian
Published in Nature genetics (01.12.1995)
Published in Nature genetics (01.12.1995)
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Journal Article
Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patients
Kavamura, M.I., Zollino, M., Lecce, R., Murdolo, M., Brunoni, D., Alchorne, M.M.A., Opitz, J.M., Neri, G.
Published in American journal of medical genetics. Part A (01.06.2003)
Published in American journal of medical genetics. Part A (01.06.2003)
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Journal Article
Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36
Thiele, H, McCann, C, van’t Padje, S, Schwabe, G C, Hennies, H C, Camera, G, Opitz, J, Laxova, R, Mundlos, S, Nürnberg, P
Published in Journal of medical genetics (01.03.2004)
Published in Journal of medical genetics (01.03.2004)
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Journal Article
"DOUBLE-MUSCLE" TRAIT IN CATTLE: A POSSIBLE MODEL FOR WIEDEMANN-BECKWITH SYNDROME
Best, L. G., Gilbert-Barness, E., Gerrard, D. E., Gendron-Fitzpatrick, A., Opitz, J. M.
Published in Fetal and pediatric pathology (01.01.2006)
Published in Fetal and pediatric pathology (01.01.2006)
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