EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients von Cohen, Jennifer L., Schrier Vergano, Samantha A., Mazzola, Sarah, Strong, Alanna, Keena, Beth, McDougall, Carey, Ritter, Alyssa, Li, Dong, Bedoukian, Emma C., Burke, Leah W., Hoffman, Amber, Zurcher, Victoria, Krantz, Ian D., Izumi, Kosuke, Bhoj, Elizabeth, Zackai, Elaine H., Deardorff, Matthew A.

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Two Cases of Preaxial Polydactyly of the Foot: Important Implications for Plastic Surgeons von Silverstein, Max L., Burke, Leah W., Laub, Donald R.

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Disclosure of Genome Sequencing Results: Are Pediatricians Ready? von Burke, Leah W

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Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation von Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.

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Health Supervision for Children and Adolescents With Marfan Syndrome von Tinkle, Brad T, Lacro, Ronald V, Burke, Leah W

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Leukodystrophies in Children: Diagnosis, Care, and Treatment von Bonkowsky, Joshua L., Keller, Stephanie

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Call for improvement in medical school training in genetics: results of a national survey von Haspel, Richard L., Genzen, Jonathan R., Wagner, Jay, Fong, Karen, Haspel, Richard L., Wilcox, Rebecca, Adem, Patricia V., Anderson, Hana, Atkinson, James B., Burke, Leah W., Joseph, Loren, LeGallo, Robin D., Lew, Madelyn, Lockwood, Christina M., Naeem, Rizwan, Rizvi, Hasan, Ortega, Julian Sanz, Shane-Carson, Kate, Sobel, Mark E., Suarez, Eric, Tafe, Laura J., Wang, Jason, Wilcox, Rebecca L.

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Utilizing RNA and outlier analysis to identify an intronic splice‐altering variant in AP4S1 in a sibling pair with progressive spastic paraplegia von McCullough, Carmel G., Szelinger, Szabolcs, Belnap, Newell, Ramsey, Keri, Schrauwen, Isabelle, Claasen, Ana M., Burke, Leah W., Siniard, Ashley L., Huentelman, Matthew J., Narayanan, Vinodh, Craig, David W.

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Management Principles for Acute Illness in Patients With Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency von McGregor, Tracy L., Berry, Susan A., Dipple, Katrina M., Hamid, Rizwan

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Congenital Hypothyroidism: Screening and Management von Rose, Susan R, Wassner, Ari J, Wintergerst, Kupper A, Yayah-Jones, Nana-Hawa, Hopkin, Robert J, Chuang, Janet, Smith, Jessica R, Abell, Katherine, LaFranchi, Stephen H

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Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation von Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.

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Familial unilateral ectopia lentis von Simon, John W., MD, Cotliar, Jeremy M, Burke, Leah W., MD

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Health Supervision for People With Achondroplasia von Hoover-Fong, Julie, Scott, Charles, Jones, Marilyn C.

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Health Supervision for Children With Neurofibromatosis Type 1 von Miller, David T, Freedenberg, Debra, Schorry, Elizabeth, Ullrich, Nicole J, Viskochil, David, Korf, Bruce R

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Health Care Supervision for Children With Williams Syndrome von Morris, Colleen A., Braddock, Stephen R., Chen, Emily, Trotter, Tracy L., Berry, Susan A., Burke, Leah W., Geleske, Timothy A., Hamid, Rizwan, Hopkin, Robert J., Introne, Wendy J., Lyons, Michael J., Scheuerle, Angela E., Stoler, Joan M.

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Health Supervision for Children and Adolescents With Down Syndrome von Bull, Marilyn J, Trotter, Tracy, Santoro, Stephanie L, Christensen, Celanie, Grout, Randall W, Burke, Leah W, Berry, Susan A, Geleske, Timothy A, Holm, Ingrid, Hopkin, Robert J, Introne, Wendy J, Lyons, Michael J, Monteil, Danielle C, Scheuerle, Angela, Stoler, Joan M, Vergano, Samantha A, Chen, Emily, Hamid, Rizwan, Downs, Stephen M, Grout, Randall W, Cunniff, Christopher, Parisi, Melissa A, Ralston, Steven J, Scott, Joan A, Shapira, Stuart K, Spire, Paul

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Congenital Hypothyroidism: Screening and Management von Rose, Susan R, Wassner, Ari J, Wintergerst, Kupper A, Yayah-Jones, Nana-Hawa, Hopkin, Robert J, Chuang, Janet, Smith, Jessica R, Abell, Katherine, LaFranchi, Stephen H

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Marshall-Smith syndrome: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities von Adam, Margaret P., Hennekam, Raoul C.M., Keppen, Laura Davis, Bull, Marilyn J., Clericuzio, Carol L., Burke, Leah W., Ormond, Kelly E., Hoyme, Eugene H.

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Front Cover, Volume 41, Issue 2 von McCullough, Carmel G., Szelinger, Szabolcs, Belnap, Newell, Ramsey, Keri, Schrauwen, Isabelle, Claasen, Ana M., Burke, Leah W., Siniard, Ashley L., Huentelman, Matthew J., Narayanan, Vinodh, Craig, David W.

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Two Cases of Preaxial Polydactyly of the Foot: Important Implications for Plastic Surgeons von Silverstein, Max L., Burke, Leah W., Laub, Donald R.

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