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There are 19669 results for: content related to: The Richieri-Costa and Pereira syndrome: Report of two Brazilian siblings and review of literature

  1. Richieri-Costa and Pereira form of acrofacial dysostosis: First description of an adult with mesomelic shortness of the lower limbs

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 12, December 2009, Pages: 2886–2888, Carla Graziadio, Rafael F.M. Rosa, Paulo R.G. Zen, José A.M. Flores and Giorgio A. Paskulin

    Version of Record online : 24 NOV 2009, DOI: 10.1002/ajmg.a.33109

  2. Richieri-costa and Pereira syndrome: Severe phenotype

    American Journal of Medical Genetics Part A

    Volume 161, Issue 8, August 2013, Pages: 1999–2003, Salmo Raskin, Marcela Souza, Mariana C. Medeiros, Mayra Manfron and Debora C. Chong e Silva

    Version of Record online : 21 JUN 2013, DOI: 10.1002/ajmg.a.35989

  3. The Richieri-Costa and Pereira form of acrofacial dysostosis: First case in a non-Brazilian infant

    American Journal of Medical Genetics

    Volume 87, Issue 5, 22 December 1999, Pages: 430–433, Elisabeth Walter-Nicolet, Anne Coëslier, Sylvie Joriot, Nadine Kacet, Alexandre Moerman and Sylvie Manouvrier-Hanu

    Version of Record online : 10 DEC 1999, DOI: 10.1002/(SICI)1096-8628(19991222)87:5<430::AID-AJMG11>3.0.CO;2-9

  4. Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome

    American Journal of Medical Genetics Part A

    Volume 122A, Issue 1, 15 September 2003, Pages: 56–58, R.L.L. Ferreira de Lima, D. Moretti-Ferreira, A. Richieri-Costa and J.C. Murray

    Version of Record online : 15 MAY 2003, DOI: 10.1002/ajmg.a.20270

  5. You have free access to this content
    Richieri-Costa–Pereira syndrome: A unique acrofacial dysostosis type. An overview of the Brazilian cases

    American Journal of Medical Genetics Part A

    Volume 155, Issue 2, February 2011, Pages: 322–331, Francine Pinheiro Favaro, Roseli Maria Zechi-Ceide, Camila Wenceslau Alvarez, Luciana P. Maximino, Luis Fernando B. B. Antunes, Antonio Richieri-Costa and Maria Leine Guion-Almeida

    Version of Record online : 22 DEC 2010, DOI: 10.1002/ajmg.a.33806

  6. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: Description of two new patients

    American Journal of Medical Genetics Part A

    Volume 122A, Issue 2, 1 October 2003, Pages: 133–138, Alfredo Tabith Jr and Cristina Guedes de Azevedo Bento-Gonçalves

    Version of Record online : 29 JUL 2003, DOI: 10.1002/ajmg.a.10227

  7. Laryngeal malformation in Richieri-Costa Pereira syndrome: New findings

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 8, August 2012, Pages: 1967–1970, Haline Coracine Miguel, Christiano Giácomo Carneiro, Alfredo Tabith Jr., Roseli Maria Zechi-Ceide and Katia Flores Genaro

    Version of Record online : 18 JUN 2012, DOI: 10.1002/ajmg.a.35421

  8. Laryngeal malformations in the Richieri-Costa and pereira form of acrofacial dysostosis

    American Journal of Medical Genetics

    Volume 66, Issue 4, 30 December 1996, Pages: 399–402, A. Tabith Jr. and C.G.A. Bento Gonçalves

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19961230)66:4<399::AID-AJMG3>3.0.CO;2-G

  9. Richieri-Costa-Pereira syndrome: expanding its phenotypic and genotypic spectrum

    Clinical Genetics

    Accepted manuscript online: 7 NOV 2017, D.R. Bertola, G. Hsia, L. Alvizi, A. Gardham, E. Wakeling, G.L. Yamamoto, R.S. Honjo, L.A.N. Oliveira, R.C. Di Francesco, B.A. Perez, C.A. Kim and M.R. Passos-Bueno

    DOI: 10.1111/cge.13169

  10. Acrofacial dysostoses: Review and report of a previously undescribed condition: The autosomal or X-linked dominant catania form of acrofacial dysostosis

    American Journal of Medical Genetics

    Volume 47, Issue 5, 1 October 1993, Pages: 660–678, John M. Opitz, Florindo Mollica, Giovanni Sorge, Gabriella Milana, Gabriella Cimino and Mario Caltabiano

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320470517

  11. Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in Brazil

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 154C, Issue 1, 15 February 2010, Pages: 149–157, Antonio Richieri-Costa and Lucilene Arilho Ribeiro

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30247

  12. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: Another affected Brazilian patient born to consanguineous parents

    American Journal of Medical Genetics

    Volume 71, Issue 2, 8 August 1997, Pages: 233–235, A. Richieri-Costa and I. L. Brandão-Almeida

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19970808)71:2<233::AID-AJMG23>3.0.CO;2-E

  13. Subtypes of frontonasal dysplasia are useful in determining clinical prognosis

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 3069–3078, E. Wu, K. Vargevik and A.M. Slavotinek

    Version of Record online : 22 OCT 2007, DOI: 10.1002/ajmg.a.31963

  14. Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: Report of 10 Brazilian male patients

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 5, May 2009, Pages: 1006–1011, Maria Leine Guion-Almeida and Antonio Richieri-Costa

    Version of Record online : 13 APR 2009, DOI: 10.1002/ajmg.a.32717

  15. Ophthalmo-acromelic syndrome: Report and review

    American Journal of Medical Genetics

    Volume 90, Issue 2, 17 January 2000, Pages: 150–154, Mustafa Tekin, Ercan Tutar, Saadet Arsan, Gülsüm Atay and Joann Bodurtha

    Version of Record online : 3 MAR 2000, DOI: 10.1002/(SICI)1096-8628(20000117)90:2<150::AID-AJMG12>3.0.CO;2-C

  16. Human facial dysostoses

    Clinical Genetics

    Volume 83, Issue 6, June 2013, Pages: 499–510, D Wieczorek

    Version of Record online : 8 APR 2013, DOI: 10.1111/cge.12123

  17. Bifurcation of the femur with tibial agenesis and additional anomalies

    American Journal of Medical Genetics Part A

    Volume 138A, Issue 1, 15 September 2005, Pages: 45–50, J.M. van de Kamp, J.J. van der Smagt, C.F.A. Bos, A. van Haeringen, P.C.W. Hogendoorn and M.H. Breuning

    Version of Record online : 12 AUG 2005, DOI: 10.1002/ajmg.a.30918

  18. Single median maxillary central incisor: New data and mutation review

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 79, Issue 8, August 2007, Pages: 573–580, Kênia B. El-Jaick, Renata F. Fonseca, Miguel A. Moreira, Márcia G. Ribeiro, Ana M. Bolognese, Sânia O. Dias, Eliane T. Pereira, Eduardo E. Castilla and Iêda M. Orioli

    Version of Record online : 21 JUN 2007, DOI: 10.1002/bdra.20380

  19. Cerebro-oculo-nasal syndrome: 13 new Brazilian cases

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 3252–3266, Maria Leine Guion-Almeida, Roseli Maria Zechi-Ceide and Antonio Richieri-Costa

    Version of Record online : 5 NOV 2007, DOI: 10.1002/ajmg.a.32090

  20. The nosology of Richieri-Costa/Guion-Almeida syndrome(s)

    American Journal of Medical Genetics Part A

    Volume 155, Issue 2, February 2011, Pages: 398–402, Marco Castori, Piero Cascone, Marco Brinelli, Giorgio Iannetti and Paola Grammatico

    Version of Record online : 22 DEC 2010, DOI: 10.1002/ajmg.a.33805