American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss von Alford, Raye L, Arnos, Kathleen S, Fox, Michelle, Lin, Jerry W, Palmer, Christina G, Pandya, Arti, Rehm, Heidi L, Robin, Nathaniel H, Scott, Daryl A, Yoshinaga-Itano, Christine

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Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay von Burnside, Rachel D., Pasion, Romela, Mikhail, Fady M., Carroll, Andrew J., Robin, Nathaniel H., Youngs, Erin L., Gadi, Inder K., Keitges, Elizabeth, Jaswaney, Vikram L., Papenhausen, Peter R., Potluri, Venkateswara R., Risheg, Hiba, Rush, Brooke, Smith, Janice L., Schwartz, Stuart, Tepperberg, James H., Butler, Merlin G.

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Defining the Clinical Spectrum of Deletion 22q11.2 von Robin, Nathaniel H., Shprintzen, Robert J.

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De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive von Tokita, Mari J., Braxton, Alicia A., Shao, Yunru, Lewis, Andrea M., Vincent, Marie, Küry, Sébastien, Besnard, Thomas, Isidor, Bertrand, Latypova, Xénia, Bézieau, Stéphane, Liu, Pengfei, Motter, Connie S., Melver, Catherine Ward, Robin, Nathaniel H., Infante, Elena M., McGuire, Marianne, El-Gharbawy, Areeg, Littlejohn, Rebecca O., McLean, Scott D., Bi, Weimin, Bacino, Carlos A., Lalani, Seema R., Scott, Daryl A., Eng, Christine M., Yang, Yaping, Schaaf, Christian P., Walkiewicz, Magdalena A.

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Lessons in genetics: Common diseases occur in patients with a genetic syndrome von Robin, Nathaniel H.

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Clinical relevance of small copy-number variants in chromosomal microarray clinical testing von Hollenbeck, Dana, Williams, Crescenda L., Drazba, Kathryn, Descartes, Maria, Korf, Bruce R., Rutledge, S. Lane, Lose, Edward J., Robin, Nathaniel H., Carroll, Andrew J., Mikhail, Fady M.

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Choose your words carefully von Robin, Nathaniel H.

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Amniotic Constriction Band: A Multidisciplinary Assessment of Etiology and Clinical Presentation von Goldfarb, Charles A, Sathienkijkanchai, Achara, Robin, Nathaniel H

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Medical students' reproductive health perspectives: Pre‐ and post‐Roe v Wade reversal von Jenkins, Morgan, Hayslip, Margaret, Bruce, Channing Freeman, Robin, Nathaniel H.

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Teaching dysmorphology in the era of genomics: new technologies, new learners von Robin, Nathaniel H

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Incidental Detection of Cancer Predisposition Gene Copy Number Variations by Array Comparative Genomic Hybridization von Hamm, J. Austin, MD, Mikhail, Fady M., MD, PhD, Hollenbeck, Dana, MPH, MS, CGC, Farmer, Meagan, MS, CGC, Robin, Nathaniel H., MD

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“Why did I choose genetics?”: A survey of current and recent medical genetics and genomics residents provides insight into recruitment efforts von Hayek, Jennifer Cassady, Blitzer, Miriam G., Robin, Nathaniel H.

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Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) von Li, Marilyn M., Tayoun, Ahmad Abou, DiStefano, Marina, Pandya, Arti, Rehm, Heidi L., Robin, Nathaniel H., Schaefer, Amanda M., Yoshinaga-Itano, Christine

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Genetic testing hearing loss: The challenge of non syndromic mimics von Gooch, Catherine, Rudy, Natasha, Smith, Richard JH, Robin, Nathaniel H.

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Genetic Testing in Cardiovascular Disease von Robin, Nathaniel H., MD, Tabereaux, Paul B., MD, MPH, Benza, Raymond, MD, Korf, Bruce R., MD, PhD

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Educating the Adolescent and Young Adult With Cystic Fibrosis About Their Reproductive Risks and Options von Staub, Milner Owens, BS, Leon, Kevin, MD, Robin, Nathaniel H., MD

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Growth parameters: the cheap and easy genetic test von Robin, Nathaniel H

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Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation von Robin, Nathaniel H., Taylor, Clare J., McDonald-McGinn, Donna M., Zackai, Elaine H., Bingham, Peter, Collins, Kevin J., Earl, Dawn, Gill, Deepak, Granata, Tiziana, Guerrini, Renzo, Katz, Naomi, Kimonis, Virginia, Lin, Jean-Pierre, Lynch, David R., Mohammed, Shehla N., Massey, Roger F., McDonald, Marie, Rogers, R. Curtis, Splitt, Miranda, Stevens, Cathy A., Tischkowitz, Marc D., Stoodley, Neil, Leventer, Richard J, Pilz, Daniela T., Dobyns, William B.

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Simultaneous osteosarcoma and renal cell carcinoma with BRCA1 mutation in a young male adult with prior oligodendroglioma von Dhir, Aditi, Li, Rong, Li, Geling, Dean, Joy, Robin, Nathaniel H., Alva, Elizabeth

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Novel de novo pathogenic variant in the NR2F2 gene in a boy with congenital heart defect and dysmorphic features von Upadia, Jariya, Gonzales, Patrick R., Robin, Nathaniel H.

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