Augmentation of the insufficient tissue bed for surgical repair of hypospadias using acellular matrix grafts: A proof of concept study von Morgante, Debora, Radford, Anna, Abbas, Syed K, Ingham, Eileen, Subramaniam, Ramnath, Southgate, Jennifer

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Translation of mechanical strain to a scalable biomanufacturing process for acellular matrix production from full thickness porcine bladders von Ward, Ashley, Morgante, Debora, Fisher, John, Ingham, Eileen, Southgate, Jennifer

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Posterior Urethral Valves: Relationship Between Vesicoureteral Reflux and Renal Function von Cozzi, Denis A, Morgante, Debora, Frediani, Simone, Iaconelli, Romina, Ceccanti, Silvia, Mele, Ermelinda, Cozzi, Francesco

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Moving toward laparoscopic pyloromyotomy: an initial Italian experience and national survey von Ceccanti, Silvia, Mele, Ermelinda, Frediani, Simone, Morgante, Debora, Iaconelli, Romina, Almenrader, Nicole, Passariello, Maurizio, Cozzi, Denis A

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Stepladder incision technique for radical excision of suprasternal thyroglossal duct remnant von Ceccanti, Silvia, Frediani, Simone, Morgante, Debora, Iaconelli, Romina, Mele, Ermelinda, Cozzi, Denis A

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Bladder Tissue Regeneration von Morgante, Debora, Southgate, Jenny

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Translation of mechanical strain to a scalable biomanufacturing process for acellular matrix production from full thickness porcine bladder von Ward, Ashley, Morgante, Debora, Fisher, John, Ingham, Eileen, Southgate, Jennifer

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Augmentation of the insufficient tissue bed for surgical repair of hypospadias using acellular matrix grafts:A proof of concept study von Morgante, Debora, Radford, Anna, Abbas, Syed K, Ingham, Eileen, Subramaniam, Ramnath, Southgate, Jennifer

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Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil von Krepischi, Ana C. V., Villela, Darine, da Costa, Silvia Souza, Mazzonetto, Patricia C., Schauren, Juliana, Migliavacca, Michele P., Milanezi, Fernanda, Santos, Juliana G., Guida, Gustavo, Guarischi-Sousa, Rodrigo, Campana, Gustavo, Kok, Fernando, Schlesinger, David, Kitajima, Joao Paulo, Campagnari, Francine, Bertola, Debora R., Vianna-Morgante, Angela M., Pearson, Peter L., Rosenberg, Carla

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Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases von Carneiro, Thaise Nr, Krepischi, Ana Cv, Costa, Silvia S, Tojal da Silva, Israel, Vianna-Morgante, Angela M, Valieris, Renan, Ezquina, Suzana Am, Bertola, Debora R, Otto, Paulo A, Rosenberg, Carla

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Skewed X-chromosome Inactivation in Women with Idiopathic Intellectual Disability is Indicative of Pathogenic Variants von Chaves, Luiza D., Carvalho, Laura M. L., Tolezano, Giovanna C., Pires, Sara F., Costa, Silvia S., de Scliar, Marília O., Giuliani, Liane de R., Bertola, Debora R., Santos-Rebouças, Cíntia B., Seo, Go Hun, Otto, Paulo A., Rosenberg, Carla, Vianna-Morgante, Angela M., Krepischi, Ana C. V.

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Clinical Characterization and Underlying Genetic Findings in Brazilian Patients with Syndromic Microcephaly Associated with Neurodevelopmental Disorders von Tolezano, Giovanna Cantini, Bastos, Giovanna Civitate, da Costa, Silvia Souza, Scliar, Marília de Oliveira, de Souza, Carolina Fischinger Moura, Van Der Linden Jr, Hélio, Fernandes, Walter Luiz Magalhães, Otto, Paulo Alberto, Vianna-Morgante, Angela M., Haddad, Luciana Amaral, Honjo, Rachel Sayuri, Yamamoto, Guilherme Lopes, Kim, Chong Ae, Rosenberg, Carla, Jorge, Alexander Augusto de Lima, Bertola, Débora Romeo, Krepischi, Ana Cristina Victorino

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Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome von Bonaldi, Adriano, Mazzeu, Juliana F., Costa, Silvia S., Honjo, Rachel S., Bertola, Débora R., Albano, Lilian M.J., Furquim, Isabel M., Kim, Chong A., Vianna‐Morgante, Angela M.

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Phenotypic and mutational spectrum of ROR2‐related Robinow syndrome von Lima, Ariadne R., Ferreira, Barbara M., Zhang, Chaofan, Jolly, Angad, Du, Haowei, White, Janson J., Dawood, Moez, Lins, Tulio C., Chiabai, Marcela A., Beusekom, Ellen, Cordoba, Mara S., Caldas Rosa, Erica C.C., Kayserili, Hulya, Kimonis, Virginia, Wu, Erica, Mellado, Cecilia, Aggarwal, Vineet, Richieri‐Costa, Antonio, Brunoni, Décio, Canó, Talyta M., Jorge, Alexander A. L., Kim, Chong A., Honjo, Rachel, Bertola, Débora R., Dandalo‐Girardi, Raissa M., Bayram, Yavuz, Gezdirici, Alper, Yilmaz‐Gulec, Elif, Gumus, Evren, Yilmaz, Gülay C., Okamoto, Nobuhiko, Ohashi, Hirofumi, Coban–Akdemir, Zeynep, Mitani, Tadahiro, Jhangiani, Shalini N., Muzny, Donna M., Regattieri, Neysa A.P., Pogue, Robert, Pereira, Rinaldo W., Otto, Paulo A., Gibbs, Richard A., Ali, Bassam R., Bokhoven, Hans, Brunner, Han G., Sutton, V. Reid, Lupski, James R., Vianna‐Morgante, Angela M., Carvalho, Claudia M. B., Mazzeu, Juliana F.

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The clinical impact of chromosomal rearrangements with breakpoints upstream of the SOX9 gene: two novel de novo balanced translocations associated with acampomelic campomelic dyspl... von Fonseca, Ana Carolina S, Bonaldi, Adriano, Bertola, Débora R, Kim, Chong A, Otto, Paulo A, Vianna-Morgante, Angela M

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Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature von Tolezano, Giovanna Cantini, Bastos, Giovanna Civitate, da Costa, Silvia Souza, Freire, Bruna Lucheze, Homma, Thais Kataoka, Honjo, Rachel Sayuri, Yamamoto, Guilherme Lopes, Passos-Bueno, Maria Rita, Koiffmann, Celia Priszkulnik, Kim, Chong Ae, Vianna-Morgante, Angela Maria, de Lima Jorge, Alexander Augusto, Bertola, Débora Romeo, Rosenberg, Carla, Krepischi, Ana Cristina Victorino

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KIF11 microdeletion is associated with microcephaly, chorioretinopathy and intellectual disability von Malvezzi, João VM, H Magalhaes, Ingrid, S Costa, Silvia, Otto, Paulo A, Rosenberg, Carla, Bertola, Debora R, LM Fernandes, Walter, Vianna-Morgante, Angela M, Krepischi, Ana CV

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Two distinct regions in 2q24.2‐q24.3 associated with idiopathic epilepsy von Krepischi, Ana Cristina Victorino, Knijnenburg, Jeroen, Bertola, Debora Romeo, Kim, Chong Ae, Pearson, Peter Lees, Bijlsma, Emilia, Szuhai, Karoly, Kok, Fernando, Vianna‐Morgante, Angela Maria, Rosenberg, Carla

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Back Cover, Volume 43, Issue 7 von Lima, Ariadne R., Ferreira, Barbara M., Zhang, Chaofan, Jolly, Angad, Du, Haowei, White, Janson J., Dawood, Moez, Lins, Tulio C., Chiabai, Marcela A., Beusekom, Ellen, Cordoba, Mara S., Caldas Rosa, Erica C.C., Kayserili, Hulya, Kimonis, Virginia, Wu, Erica, Mellado, Cecilia, Aggarwal, Vineet, Richieri‐Costa, Antonio, Brunoni, Décio, Canó, Talyta M., Jorge, Alexander A. L., Kim, Chong A., Honjo, Rachel, Bertola, Débora R., Dandalo‐Girardi, Raissa M., Bayram, Yavuz, Gezdirici, Alper, Yilmaz‐Gulec, Elif, Gumus, Evren, Yilmaz, Gülay C., Okamoto, Nobuhiko, Ohashi, Hirofumi, Coban–Akdemir, Zeynep, Mitani, Tadahiro, Jhangiani, Shalini N., Muzny, Donna M., Regattieri, Neysa A.P., Pogue, Robert, Pereira, Rinaldo W., Otto, Paulo A., Gibbs, Richard A., Ali, Bassam R., Bokhoven, Hans, Brunner, Han G., Sutton, V. Reid, Lupski, James R., Vianna‐Morgante, Angela M., Carvalho, Claudia M. B., Mazzeu, Juliana F.

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Investigating Genetic Factors Contributing to Variable Expressivity of Class I 17p13.3 Microduplication von Tolezano, Giovanna Cantini, da Costa, Silvia Souza, Scliar, Marília de Oliveira, Fernandes, Walter Luis Magalhães, Otto, Paulo Alberto, Bertola, Débora Romeo, Rosenberg, Carla, Vianna-Morgante, Angela Maria, Krepischi, Ana Cristina Victorino

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