A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay von Eichler, Evan E, Girirajan, Santhosh, Rosenfeld, Jill A, Cooper, Gregory M, Antonacci, Francesca, Siswara, Priscillia, Itsara, Andy, Vives, Laura, Walsh, Tom, McCarthy, Shane E, Baker, Carl, Mefford, Heather C, Kidd, Jeffrey M, Browning, Sharon R, Browning, Brian L, Dickel, Diane E, Levy, Deborah L, Ballif, Blake C, Platky, Kathryn, Farber, Darren M, Gowans, Gordon C, Wetherbee, Jessica J, Asamoah, Alexander, Weaver, David D, Mark, Paul R, Dickerson, Jennifer, Garg, Bhuwan P, Ellingwood, Sara A, Smith, Rosemarie, Banks, Valerie C, Smith, Wendy, McDonald, Marie T, Hoo, Joe J, French, Beatrice N, Hudson, Cindy, Johnson, John P, Ozmore, Jillian R, Moeschler, John B, Surti, Urvashi, Escobar, Luis F, El-Khechen, Dima, Gorski, Jerome L, Kussmann, Jennifer, Salbert, Bonnie, Lacassie, Yves, Biser, Alisha, McDonald-McGinn, Donna M, Zackai, Elaine H, Deardorff, Matthew A, Shaikh, Tamim H, Haan, Eric, Friend, Kathryn L, Fichera, Marco, Romano, Corrado, Gécz, Jozef, DeLisi, Lynn E, Sebat, Jonathan, King, Mary-Claire, Shaffer, Lisa G

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FG syndrome, an X-linked multiple congenital anomaly syndrome: The clinical phenotype and an algorithm for diagnostic testing von Clark, Robin Dawn, Graham, John M, Friez, Michael J, Hoo, Joe J, Jones, Kenneth Lyons, McKeown, Carole, Moeschler, John B, Raymond, F Lucy, Rogers, R Curtis, Schwartz, Charles E, Battaglia, Agatino, Lyons, Michael J, Stevenson, Roger E

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Difficulty in Recognizing Multiple Sulfatase Deficiency in an Infant von Santos, Roberto P, Hoo, Joe J

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"Zwilling" versus "Tai Chi" configuration of double-sized ring chromosome von Hoo, Joe J., Stein, Constance K.

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Familial hyper- and hypopigmentation with age-related pattern change von Hoo, Joe J., Shrimpton, Antony E.

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Is brachydactyly type Ballard a variant of brachydactyly type E? von Jensen, Kimberly, Hoo, Joe J.

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Two sibs with brachyolmia type Hobaek: Five year follow‐up through puberty von Hoo, Joe J., Oliphant, Michael

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Succinate dehydrogenase deficiency associated with dilated cardiomyopathy and ventricular noncompaction von DAVILI, Zurab, JOHAR, Sandeep, HUGHES, Colleen, KVESELIS, Daniel, HOO, Joe

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Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype von Shrimpton, AE, Braddock, BR, Thomson, LL, Stein, CK, Hoo, JJ

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Deletions flanked by breakpoints 3 and 4 on 15p13 may contribute to abnormal phenotypes von ROSENFELD, Jill A, STEPHENS, Lindsey E, MERRION, Katrina, MENDOZA-LONDONO, Roberto, DUPUIS, Lucie, SCHULTZ, Roger, TORCHIA, Beth, SAHOO, Trilochan, BEJJANI, Bassem, WEAVER, David D, SHAFFER, Lisa G, COPPINGER, Justine, BALLIF, Blake C, HOO, Joe J, FRENCH, Beatrice N, BANKS, Valerie C, SMITH, Wendy E, MANCHESTER, David, TSAI, Anne Chun-Hui

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A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay von Girirajan, Santhosh, Rosenfeld, Jill A., Cooper, Gregory M., Antonacci, Francesca, Siswara, Priscillia, Itsara, Andy, Vives, Laura, Walsh, Tom, McCarthy, Shane E., Baker, Carl, Mefford, Heather C., Kidd, Jeffrey M., Browning, Sharon R., Browning, Brian L., Dickel, Diane E., Levy, Deborah L., Ballif, Blake C., Platky, Kathryn, Farber, Darren M., Gowans, Gordon C., Wetherbee, Jessica J., Asamoah, Alexander, Weaver, David D., Mark, Paul R., Dickerson, Jennifer, Garg, Bhuwan P., Ellingwood, Sara A., Smith, Rosemarie, Banks, Valerie C., Smith, Wendy, McDonald, Marie T., Hoo, Joe J., French, Beatrice N., Hudson, Cindy, Johnson, John P., Ozmore, Jillian R., Moeschler, John B., Surti, Urvashi, Escobar, Luis F., El-Kechen, Dima, Gorski, Jerome L., Kussman, Jennifer, Salbert, Bonnie, Lacassie, Yves, Biser, Alisha, McDonald-McGinn, Donna M., Zackai, Elaine H., Deardorff, Matthew A., Shaikh, Tamim H., Haan, Eric, Friend, Kathryn L., Fichera, Marco, Romano, Corrado, Gécz, Jozef, deLisi, Lynn E., Sebat, Jonathan, King, Mary-Claire, Shaffer, Lisa G., Eichler, Evan E.

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Molecular Analysis of 9p Deletions Associated with XY Sex Reversal: Refining the Localization of a Sex-Determining Gene to the Tip of the Chromosome von Guioli, Silvana, Schmitt, Karin, Critcher, Ricky, Bouzyk, Mark, Spurr, Nigel K., Ogata, Tsutomu, Hoo, Joe J., Pinsky, Leonard, Gimelli, Giorgio, Pasztor, Linda, Goodfellow, Peter N.

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Acupressure for hyperemesis gravidarum von Hoo, Joe J.

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Letter to the Editor: Determination of Brain Type Creatine Kinase for Diagnosis of Perinatal Asphyxia-Choice of Method von Hoo, Joe J, Werner Goedde, H

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β-Glucuronidase P408S, P415L mutations : evidence that both mutations combine to produce an MPS VII allele in certain Mexican patients von ISLAM, M. R, VERVOORT, R, LISSSENS, W, HOO, J. J, VALENTINO, L. A, SLY, W. S

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Possible Teratogenicity of Sulfasalazine von Hoo, J J, Hadro, T A, Von Behren, P

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Congenital central hypoventilation syndrome: Inheritance and relation to sudden infant death syndrome von Weese-Mayer, Debra E., Silvestri, Jean M., Marazita, Mary L., Hoo, Joe J.

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Is brachydactyly type Ballard a variant of brachydactyly type E? von Jensen, Kimberly, Hoo, Joe J

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"Zwilling" versus "Tai Chi" configuration of double-sized ring chromosome von Hoo, Joe J, Stein, Constance K

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The aarskog (facio-digito-genital) syndrome von Hoo, Joe-Jie

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