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Original Article

Prenatal assessment of arthrogryposis. A review of the literature

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Pages 32-36 | Received 05 Jan 2010, Accepted 25 Feb 2010, Published online: 23 Jun 2010

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Juan Parra, Laura Alias, Eva Also-Rallo, Rebeca Martínez-Hernández, Raquel Senosiain, Carmen Medina, Obdulia Alejos, Noelia Rams, María Amenedo, Filomena Ormo, María Jesús Barceló, Joaquim Calaf, Montserrat Baiget, Sara Bernal & Eduardo F. Tizzano. (2012) Evaluation of fetal nuchal translucency in 98 pregnancies at risk for severe spinal muscular atrophy: possible relevance of the SMN2 copy number. The Journal of Maternal-Fetal & Neonatal Medicine 25:8, pages 1246-1249.
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Articles from other publishers (11)

Daniele Di Mascio, Danilo Buca, Asma Khalil, Giuseppe Rizzo, Alexander Makatsariya, Filomena Sileo, Marco Liberati, Pierluigi Benedetti Panici, Ganesh Acharya & Francesco D'Antonio. (2019) Outcome of isolated fetal talipes: A systematic review and meta‐analysis. Acta Obstetricia et Gynecologica Scandinavica 98:11, pages 1367-1377.
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Isabel Filges, Sevgi Tercanli & Judith G. Hall. (2019) Fetal arthrogryposis: Challenges and perspectives for prenatal detection and management. American Journal of Medical Genetics Part C: Seminars in Medical Genetics 181:3, pages 327-336.
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Fernanda Blaudt C. Marques, Liliane Siqueira de Morais, Luciana Rougemont Squeff, Margareth Maria Gomes de Souza & Ana Maria Bolognese. (2019) Escobar Syndrome—An Multidisciplinary Approach for an Excellent Outcome With 3 Years of Follow-Up. The Cleft Palate-Craniofacial Journal 56:7, pages 970-977.
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Bin Wang, Wei Wang & Feng Ni. 2017. Congenital Deformities of the Hand and Upper Limb. Congenital Deformities of the Hand and Upper Limb 71 94 .
Harold ChenHarold Chen. 2017. Atlas of Genetic Diagnosis and Counseling. Atlas of Genetic Diagnosis and Counseling 179 198 .
N. Dohrn, V.Q. Le, A. Petersen, P. Skovbo, I.S. Pedersen, A. Ernst, H. Krarup & M.B. Petersen. (2015) ECEL1 mutation causes fetal arthrogryposis multiplex congenita . American Journal of Medical Genetics Part A 167:4, pages 731-743.
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Harold ChenHarold Chen. 2014. Atlas of Genetic Diagnosis and Counseling. Atlas of Genetic Diagnosis and Counseling 1 21 .
M. Inbar-Feigenberg, N. Meirowitz, D. Nanda, A. Toi, N. Okun & D. Chitayat. (2014) Beals syndrome (congenital contractural arachnodactyly): prenatal ultrasound findings and molecular analysis. Ultrasound in Obstetrics & Gynecology 44:4, pages 486-490.
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Robin L. Bissinger & Frances R. Koch. (2014) Nonlethal Multiple Pterygium Syndrome. Advances in Neonatal Care 14:1, pages 24-29.
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Gabriele Tonni & Mario Lituania. (2013) Arthrogryposis multiplex congenita-like syndrome associated with median cleft lip and palates: First prenatally detected case. Congenital Anomalies 53:3, pages 137-140.
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Stefan Franz Nemec, Ursula Nemec, Peter C. Brugger, Dieter Bettelheim, Siegfried Rotmensch, John M. GrahamJr.Jr., David L. Rimoin & Daniela Prayer. (2012) MR imaging of the fetal musculoskeletal system. Prenatal Diagnosis 32:3, pages 205-213.
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