Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Intellectual Disability and SMC1A[original query] |
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Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism. Journal of medical genetics 2014 Oct 51 (10): 659-68. Ansari Morad, Poke Gemma, Ferry Quentin, Williamson Kathleen, Aldridge Roland, Meynert Alison M, Bengani Hemant, Chan Cheng Yee, Kayserili Hülya, Avci Sahin, Hennekam Raoul C M, Lampe Anne K, Redeker Egbert, Homfray Tessa, Ross Alison, Falkenberg Smeland Marie, Mansour Sahar, Parker Michael J, Cook Jacqueline A, Splitt Miranda, Fisher Richard B, Fryer Alan, Magee Alex C, Wilkie Andrew, Barnicoat Angela, Brady Angela F, Cooper Nicola S, Mercer Catherine, Deshpande Charu, Bennett Christopher P, Pilz Daniela T, Ruddy Deborah, Cilliers Deirdre, Johnson Diana S, Josifova Dragana, Rosser Elisabeth, Thompson Elizabeth M, Wakeling Emma, Kinning Esther, Stewart Fiona, Flinter Frances, Girisha Katta M, Cox Helen, Firth Helen V, Kingston Helen, Wee Jamie S, Hurst Jane A, Clayton-Smith Jill, Tolmie John, Vogt Julie, Tatton-Brown Katrina, Chandler Kate, Prescott Katrina, Wilson Louise, Behnam Mahdiyeh, McEntagart Meriel, Davidson Rosemarie, Lynch Sally-Ann, Sisodiya Sanjay, Mehta Sarju G, McKee Shane A, Mohammed Shehla, Holden Simon, Park Soo-Mi, Holder Susan E, Harrison Victoria, McConnell Vivienne, Lam Wayne K, Green Andrew J, Donnai Dian, Bitner-Glindzicz Maria, Donnelly Deirdre E, Nellåker Christoffer, Taylor Martin S, FitzPatrick David |
Next-generation sequencing in X-linked intellectual disability. European journal of human genetics : EJHG 2015 Feb . Tzschach Andreas, Grasshoff Ute, Beck-Woedl Stefanie, Dufke Claudia, Bauer Claudia, Kehrer Martin, Evers Christina, Moog Ute, Oehl-Jaschkowitz Barbara, Di Donato Nataliya, Maiwald Robert, Jung Christine, Kuechler Alma, Schulz Solveig, Meinecke Peter, Spranger Stephanie, Kohlhase Jürgen, Seidel Jörg, Reif Silke, Rieger Manuela, Riess Angelika, Sturm Marc, Bickmann Julia, Schroeder Christopher, Dufke Andreas, Riess Olaf, Bauer Pet |
Behavioral Phenotype and Autism Spectrum Disorders in Cornelia de Lange Syndrome. Mental illness 2015 Sep 7 (2): 5988. Parisi Lucia, Di Filippo Teresa, Roccella Miche |
Cornelia de Lange syndrome in diverse populations. American journal of medical genetics. Part A 2019 1 179 (2): 150-158. Dowsett Leah, Porras Antonio R, Kruszka Paul, Davis Brandon, Hu Tommy, Honey Engela, Badoe Eben, Thong Meow-Keong, Leon Eyby, Girisha Katta M, Shukla Anju, Nayak Shalini S, Shotelersuk Vorasuk, Megarbane Andre, Phadke Shubha, Sirisena Nirmala D, Dissanayake Vajira H W, Ferreira Carlos R, Kisling Monisha S, Tanpaiboon Pranoot, Uwineza Annette, Mutesa Leon, Tekendo-Ngongang Cedrik, Wonkam Ambroise, Fieggen Karen, Batista Leticia Cassimiro, Moretti-Ferreira Danilo, Stevenson Roger E, Prijoles Eloise J, Everman David, Clarkson Kate, Worthington Jessica, Kimonis Virginia, Hisama Fuki, Crowe Carol, Wong Paul, Johnson Kisha, Clark Robin D, Bird Lynne, Masser-Frye Diane, McDonald Marie, Willems Patrick, Roeder Elizabeth, Saitta Sulgana, Anyane-Yeoba Kwame, Demmer Laurie, Hamajima Naoki, Stark Zornitza, Gillies Greta, Hudgins Louanne, Dave Usha, Shalev Stavit, Siu Victoria, Ades Ann, Dubbs Holly, Raible Sarah, Kaur Maninder, Salzano Emanuela, Jackson Laird, Deardorff Matthew, Kline Antonie, Summar Marshall, Muenke Maximilian, Linguraru Marius George, Krantz Ian |
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- Page last updated:May 06, 2024
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