Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss von Simpson, Michael A, Irving, Melita D, Asilmaz, Esra, Gray, Mary J, Dafou, Dimitra, Elmslie, Frances V, Mansour, Sahar, Holder, Sue E, Brain, Caroline E, Burton, Barbara K, Kim, Katherine H, Pauli, Richard M, Aftimos, Salim, Stewart, Helen, Kim, Chong Ae, Holder-Espinasse, Muriel, Robertson, Stephen P, Drake, William M, Trembath, Richard C

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The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1 von Hanson, Dan, Murray, Philip G., Sud, Amit, Temtamy, Samia A., Aglan, Mona, Superti-Furga, Andrea, Holder, Sue E., Urquhart, Jill, Hilton, Emma, Manson, Forbes D.C., Scambler, Peter, Black, Graeme C.M., Clayton, Peter E.

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Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder von Poot, Martin, Beyer, Vera, Schwaab, Ira, Damatova, Natalja, van’t Slot, Ruben, Prothero, Jo, Holder, Sue E., Haaf, Thomas

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De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith... von Vetrini, Francesco, McKee, Shane, Rosenfeld, Jill A, Suri, Mohnish, Lewis, Andrea M, Nugent, Kimberly Margaret, Roeder, Elizabeth, Littlejohn, Rebecca O, Holder, Sue, Zhu, Wenmiao, Alaimo, Joseph T, Graham, Brett, Harris, Jill M, Gibson, James B, Pastore, Matthew, McBride, Kim L, Komara, Makanko, Al-Gazali, Lihadh, Al Shamsi, Aisha, Fanning, Elizabeth A, Wierenga, Klaas J, Scott, Daryl A, Ben-Neriah, Ziva, Meiner, Vardiella, Cassuto, Hanoch, Elpeleg, Orly, Holder, Jr, J Lloyd, Burrage, Lindsay C, Seaver, Laurie H, Van Maldergem, Lionel, Mahida, Sonal, Soul, Janet S, Marlatt, Margaret, Matyakhina, Ludmila, Vogt, Julie, Gold, June-Anne, Park, Soo-Mi, Varghese, Vinod, Lampe, Anne K, Kumar, Ajith, Lees, Melissa, Holder-Espinasse, Muriel, McConnell, Vivienne, Bernhard, Birgitta, Blair, Ed, Harrison, Victoria, Muzny, Donna M, Gibbs, Richard A, Elsea, Sarah H, Posey, Jennifer E, Bi, Weimin, Lalani, Seema, Xia, Fan, Yang, Yaping, Eng, Christine M, Lupski, James R, Liu, Pengfei

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CHRNG genotype–phenotype correlations in the multiple pterygium syndromes von Vogt, Julie, Morgan, Neil V, Rehal, Pauline, Faivre, Laurence, Brueton, Louise A, Becker, Kristin, Fryns, Jean-Pierre, Holder, Sue, Islam, Lily, Kivuva, Emma, Lynch, Sally Ann, Touraine, Renaud, Wilson, Louise C, MacDonald, Fiona, Maher, Eamonn R

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Molecular study of 33 families with Fraser syndrome new data and mutation review von van Haelst, M.M., Maiburg, M., Baujat, G., Jadeja, S., Monti, E., Bland, E., Pearce, K., Hennekam, R.C., Scambler, P.J.

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Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with simila... von Vetrini, Francesco, McKee, Shane, Rosenfeld, Jill A, Suri, Mohnish, Lewis, Andrea M, Nugent, Kimberly Margaret, Roeder, Elizabeth, Littlejohn, Rebecca O, Holder, Sue, Zhu, Wenmiao, Alaimo, Joseph T, Graham, Brett, Harris, Jill M, Gibson, James B, Pastore, Matthew, McBride, Kim L, Komara, Makanko, Al-Gazali, Lihadh, Al Shamsi, Aisha, Fanning, Elizabeth A, Wierenga, Klaas J, Scott, Daryl A, Ben-Neriah, Ziva, Meiner, Vardiella, Cassuto, Hanoch, Elpeleg, Orly, Lloyd Holder, Jr, J, Burrage, Lindsay C, Seaver, Laurie H, Van Maldergem, Lionel, Mahida, Sonal, Soul, Janet S, Marlatt, Margaret, Matyakhina, Ludmila, Vogt, Julie, Gold, June-Anne, Park, Soo-Mi, Varghese, Vinod, Lampe, Anne K, Kumar, Ajith, Lees, Melissa, Holder-Espinasse, Muriel, McConnell, Vivienne, Bernhard, Birgitta, Blair, Ed, Harrison, Victoria, Muzny, Donna M, Gibbs, Richard A, Elsea, Sarah H, Posey, Jennifer E, Bi, Weimin, Lalani, Seema, Xia, Fan, Yang, Yaping, Eng, Christine M, Lupski, James R, Liu, Pengfei

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Fraser syndrome: A clinical study of 59 cases and evaluation of diagnostic criteria von van Haelst, Mieke M., Scambler, Peter J., Hennekam, Raoul C.M.

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CHRNG genotype-phenotype correlations in the multiple pterygium syndromes von Vogt, Julie, Morgan, Neil V, Rehal, Pauline, Faivre, Laurence, Brueton, Louise A, Becker, Kristin, Fryns, Jean-Pierre, Holder, Sue, Islam, Lily, Kivuva, Emma, Lynch, Sally Ann, Touraine, Renaud, Wilson, Louise C, Macdonald, Fiona, Maher, Eamonn R

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Dear reader von Holder, Sue

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Belwin Contest Winners, Books 1, 2, 3 and 4, Original Piano Solos from the Libraries of Belwin-Mills and Summy-Birchard von Holder, Sue H.

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Dear Reader von Finley, Joy, Holder, Sue

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The First Term at the Piano: 18 Elementary Pieces for Piano von Holder, Sue H.

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Music Review: "The First Term at the Piano: 18 Elementary Pieces for Piano," by Bela Bartok, edited by Monika Twelsiek von Holder, Sue H

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Contest Winners for Three, piano trios from the Alfred, Belwin and Myklas Libraries, Books 1-5 von Holder, Sue H.

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Contest Winners for Three, piano trios from the Alfred, Belwin and Myklas Libraries von Holder, Sue H

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Hereditary hearing loss and its syndromes Robert J. Gorlin, Helen V. Toriello, and M. Michael J. Cohen, Jr. New York: Oxford University Press, 1995, 457 pp von Holder, Sue

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Racial Microaggressions in Everyday Life: Implications for Clinical Practice von Sue, Derald Wing, Capodilupo, Christina M, Torino, Gina C, Bucceri, Jennifer M, Holder, Aisha M. B, Nadal, Kevin L, Esquilin, Marta

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Racial Microaggressions in the Life Experience of Black Americans von Sue, Derald Wing, Capodilupo, Christina M, Holder, Aisha M. B

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Genome-wide functional analysis reveals key roles for kinesins in the mammalian and mosquito stages of the malaria parasite life cycle von Zeeshan, Mohammad, Rashpa, Ravish, Ferguson, David J P, Abel, Steven, Chahine, Zeinab, Brady, Declan, Vaughan, Sue, Moores, Carolyn A, Le Roch, Karine G, Brochet, Mathieu, Holder, Anthony A, Tewari, Rita

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