Erratum: In the article by Gene S. Fisch, entitled "Nosology and Epidemiology in Autism: Classification Counts," in. American Journal of Medical Genetics Part C (Seminars in Medical Genetics) 160C:91-103 10.1002/ajmg.c.31325 (2012) by Fisch, Gene S.

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Barth syndrome by Jefferies, John L.

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The 2017 international classification of the Ehlers–Danlos syndromes by Malfait, Fransiska, Francomano, Clair, Byers, Peter, Belmont, John, Berglund, Britta, Black, James, Bloom, Lara, Bowen, Jessica M., Brady, Angela F., Burrows, Nigel P., Castori, Marco, Cohen, Helen, Colombi, Marina, Demirdas, Serwet, De Backer, Julie, De Paepe, Anne, Fournel‐Gigleux, Sylvie, Frank, Michael, Ghali, Neeti, Giunta, Cecilia, Grahame, Rodney, Hakim, Alan, Jeunemaitre, Xavier, Johnson, Diana, Juul‐Kristensen, Birgit, Kapferer‐Seebacher, Ines, Kazkaz, Hanadi, Kosho, Tomoki, Lavallee, Mark E., Levy, Howard, Mendoza‐Londono, Roberto, Pepin, Melanie, Pope, F. Michael, Reinstein, Eyal, Robert, Leema, Rohrbach, Marianne, Sanders, Lynn, Sobey, Glenda J., Van Damme, Tim, Vandersteen, Anthony, van Mourik, Caroline, Voermans, Nicol, Wheeldon, Nigel, Zschocke, Johannes, Tinkle, Brad

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A framework for the classification of joint hypermobility and related conditions by Castori, Marco, Tinkle, Brad, Levy, Howard, Grahame, Rodney, Malfait, Fransiska, Hakim, Alan

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Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history by Tinkle, Brad, Castori, Marco, Berglund, Britta, Cohen, Helen, Grahame, Rodney, Kazkaz, Hanadi, Levy, Howard

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Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome by Byers, Peter H., Belmont, John, Black, James, De Backer, Julie, Frank, Michael, Jeunemaitre, Xavier, Johnson, Diana, Pepin, Melanie, Robert, Leema, Sanders, Lynn, Wheeldon, Nigel

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The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine by Stoll, Katie, Kubendran, Shobana, Cohen, Stephanie A.

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Somatic overgrowth disorders of the PI3K/AKT/mTOR pathway & therapeutic strategies by Keppler-Noreuil, Kim M., Parker, Victoria E.R., Darling, Thomas N., Martinez-Agosto, Julian A.

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Neurological and spinal manifestations of the Ehlers–Danlos syndromes by Henderson, Fraser C., Austin, Claudiu, Benzel, Edward, Bolognese, Paolo, Ellenbogen, Richard, Francomano, Clair A., Ireton, Candace, Klinge, Petra, Koby, Myles, Long, Donlin, Patel, Sunil, Singman, Eric L., Voermans, Nicol C.

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Measurement properties of clinical assessment methods for classifying generalized joint hypermobility—A systematic review by Juul‐Kristensen, Birgit, Schmedling, Karoline, Rombaut, Lies, Lund, Hans, Engelbert, Raoul H. H.

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The Ehlers–Danlos syndromes, rare types by Brady, Angela F., Demirdas, Serwet, Fournel‐Gigleux, Sylvie, Ghali, Neeti, Giunta, Cecilia, Kapferer‐Seebacher, Ines, Kosho, Tomoki, Mendoza‐Londono, Roberto, Pope, Michael F., Rohrbach, Marianne, Van Damme, Tim, Vandersteen, Anthony, van Mourik, Caroline, Voermans, Nicol, Zschocke, Johannes, Malfait, Fransiska

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Genetic counseling globally: Where are we now? by Ormond, Kelly E., Laurino, Mercy Ygoña, Barlow‐Stewart, Kristine, Wessels, Tina‐Marié, Macaulay, Shelley, Austin, Jehannine, Middleton, Anna

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Ehlers–Danlos syndrome, classical type by Bowen, Jessica M., Sobey, Glenda J., Burrows, Nigel P., Colombi, Marina, Lavallee, Mark E., Malfait, Fransiska, Francomano, Clair A.

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Genetics of cleft lip and cleft palate by Leslie, Elizabeth J., Marazita, Mary L.

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Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment by Linglart, Léa, Gelb, Bruce D.

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Genotype–phenotype correlates in Joubert syndrome: A review by Gana, Simone, Serpieri, Valentina, Valente, Enza Maria

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Pain management in the Ehlers–Danlos syndromes by Chopra, Pradeep, Tinkle, Brad, Hamonet, Claude, Brock, Isabelle, Gompel, Anne, Bulbena, Antonio, Francomano, Clair

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22q11.2 deletion syndrome and congenital heart disease by Goldmuntz, Elizabeth

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The epidemiology of sex chromosome abnormalities by Berglund, Agnethe, Stochholm, Kirstine, Gravholt, Claus Højbjerg

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PG4KDS: A model for the clinical implementation of pre-emptive pharmacogenetics by Hoffman, James M., Haidar, Cyrine E., Wilkinson, Mark R., Crews, Kristine R., Baker, Donald K., Kornegay, Nancy M., Yang, Wenjian, Pui, Ching-Hon, Reiss, Ulrike M., Gaur, Aditya H., Howard, Scott C., Evans, William E., Broeckel, Ulrich, Relling, Mary V.

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