The lethal multiple pterygium syndromes. [Am J Med Genet. 1984] - PubMed

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Brief clinical report: lethal multiple pterygium syndrome in an 18-week fetus with hydrops. [Am J Med Genet. 1984]
Brief clinical report: lethal multiple pterygium syndrome in an 18-week fetus with hydrops.
Isaacson G, Gargus JJ, Mahoney MJ. Am J Med Genet. 1984 Apr; 17(4):835-9.
Lethal multiple pterygium syndrome. [Am J Med Genet. 1984]
Lethal multiple pterygium syndrome.
Van Regemorter N, Wilkin P, Englert Y, El Khazen N, Alexander S, Rodesch F, Milaire J. Am J Med Genet. 1984 Apr; 17(4):827-34.
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome. [Am J Med Genet. 1984]
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome.
Chen H, Immken L, Lachman R, Yang S, Rimoin DL, Rightmire D, Eteson D, Stewart F, Beemer FA, Opitz JM. Am J Med Genet. 1984 Apr; 17(4):809-26.
Review [Skin plicae and syndromes with pterygium]. [G Ital Dermatol Venereol. 1988]
Review [Skin plicae and syndromes with pterygium].
Micali GP, Rizzo R, Di Forti F, Pavone L. G Ital Dermatol Venereol. 1988 Dec; 123(12):643-8.
Review Lethal multiple pterygium syndrome in four male fetuses in a family: evidence for an X-linked recessive subtype? [Am J Med Genet. 1999]
Review Lethal multiple pterygium syndrome in four male fetuses in a family: evidence for an X-linked recessive subtype?
Meyer-Cohen J, Dillon A, Pai GS, Conradi S. Am J Med Genet. 1999 Jan 1; 82(1):97-9.

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Cited by 5 PubMed Central articles

Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. [Am J Hum Genet. 2008]
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders.
Michalk A, Stricker S, Becker J, Rupps R, Pantzar T, Miertus J, Botta G, Naretto VG, Janetzki C, Yaqoob N, et al. Am J Hum Genet. 2008 Feb; 82(2):464-76.
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients. [Am J Hum Genet. 2008]
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients.
Vogt J, Harrison BJ, Spearman H, Cossins J, Vermeer S, ten Cate LN, Morgan NV, Beeson D, Maher ER. Am J Hum Genet. 2008 Jan; 82(1):222-7.
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome. [Am J Hum Genet. 2006]
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome.
Morgan NV, Brueton LA, Cox P, Greally MT, Tolmie J, Pasha S, Aligianis IA, van Bokhoven H, Marton T, Al-Gazali L, et al. Am J Hum Genet. 2006 Aug; 79(2):390-5. Epub 2006 Jun 20.

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The lethal multiple pterygium syndromes.
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