Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?
Nowaczyk, M.J.M., Thompson, B.A., Zeesman, S., Moog, U., Sanchez-Lara, P.A., Magoulas, P.L., Falk, R.E., Hoover-Fong, J.E., Batista, D.A.S., Amudhavalli, S.M., White, S.M., Graham, G.E., Rauen, K.A.
Published in Clinical genetics (01.02.2014)
Published in Clinical genetics (01.02.2014)
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Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care
Sawyer, S.L., Hartley, T., Dyment, D.A., Beaulieu, C.L., Schwartzentruber, J., Smith, A., Bedford, H.M., Bernard, G., Bernier, F.P., Brais, B., Bulman, D.E., Warman Chardon, J., Chitayat, D., Deladoëy, J., Fernandez, B.A., Frosk, P., Geraghty, M.T., Gerull, B., Gibson, W., Gow, R.M., Graham, G.E., Green, J.S., Heon, E., Horvath, G., Innes, A.M., Jabado, N., Kim, R.H., Koenekoop, R.K., Khan, A., Lehmann, O.J., Mendoza-Londono, R., Michaud, J.L., Nikkel, S.M., Penney, L.S., Polychronakos, C., Richer, J., Rouleau, G.A., Samuels, M.E., Siu, V.M., Suchowersky, O., Tarnopolsky, M.A., Yoon, G., Zahir, F.R., Majewski, J., Boycott, K.M.
Published in Clinical genetics (01.03.2016)
Published in Clinical genetics (01.03.2016)
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Application of Hereditary Renal Cell Carcinoma Risk Criteria to a Large Prospective Database
Kushnir, I., Kirk, L., Mallick, R., Kim, R.H., Graham, G.E., Breau, R.H., Lattouf, J.-B., Violette, P.D., Pautler, S.E., Care, M., Kapoor, A., Jewett, M.A.S., Wood, L., Tanguay, S., Heng, D.Y.C., Basappa, N.S., So, A., Pouliot, F., Reaume, N.M.
Published in Clinical oncology (Royal College of Radiologists (Great Britain)) (01.01.2020)
Published in Clinical oncology (Royal College of Radiologists (Great Britain)) (01.01.2020)
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Partial Monosomy 12p and Ring Chromosome 12 Mosaicism in a Male with Developmental Delay and Mild Dysmorphism
Yee, H.A., Chemos, J.E., Veale, P.M., Clarke, M.E., Graham, G.E.
Published in Genetics in medicine (01.01.2000)
Published in Genetics in medicine (01.01.2000)
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A New Variation on an Old Theme: Subtleties of the Smith-Lemli-Opitz Syndrome (RSH/SLOS)
Yoon, G., Nezarati, M.M, Fung, E., Snyder, F.F., Graham, G.E.
Published in Genetics in medicine (01.01.1999)
Published in Genetics in medicine (01.01.1999)
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Design and test results of a transition radiation detector for a Fermilab fixed target rare kaon decay experiment
Graham, G.E., Solomey, N., Wah, Y.W., Zimmerman, E.D., Daum, M., Hsiung, Y.B., Krider, J.C., Ramberg, E.J.
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment (11.12.1995)
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment (11.12.1995)
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Search for the decay [formula omitted]
Graham, G.E., Barker, A.R., Briere, R.A., Gibbons, L.K., Makoff, G., Papadimitriou, V., Patterson, J.R., Somalwar, S.V., Wah, Y.W., Winstein, B., Winston, R., Yamamoto, H., Swallow, E.C., Bock, G.J., Coleman, R., Enagonio, J., Hsiung, Y.B., Ramberg, E., Stanfield, K., Tschirhart, R., Yamanaka, T., Gollin, G.D., Karlsson, M., Debu, P., Peyaud, B., Turlay, R., Vallage, B.
Published in Physics letters. B (01.11.1992)
Published in Physics letters. B (01.11.1992)
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King syndrome: further clinical variability and review of the literature
Graham, G E, Silver, K, Arlet, V, Der Kaloustian, V M
Published in American journal of medical genetics (07.07.1998)
Published in American journal of medical genetics (07.07.1998)
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