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Hecht syndrome
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- ... disorder. Arthrogyroposis, distal, type 9 Beals syndrome Beals-Hecht syndrome CCA Contractural arachnodactyly, congenital DA9 Distal arthrogyropsis type ...
- ... SYNDROME PubMed Hall CR, Wu Y, Shaffer LG, Hecht JT. Familial case of Potocki-Shaffer syndrome associated with microdeletion of EXT2 and ALX4. Clin ... Sue WC, Sheffield LJ, Irons M, Gomez EG, Hecht JT, Potocki L, Shaffer LG. ... involved in Potocki-Shaffer syndrome. Eur J Hum Genet. 2005 May;13(5): ...
- ... or Free article on PubMed Central Li FP, Hecht F, Kaiser-McCaw B, Baranko PV, Potter NU. Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and ...
- ... Kruger U, Zhu N, Kinoshita T, Mundlos S, Hecht J, Robinson PN, Horn D. PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome. Am J Hum Genet. 2013 Apr 4;92( ...
- ... Thiele H, Nurnberg P, Yigit G, Jager M, Hecht J, Kruger U, Mielke T, Krawitz ... Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. Am ...
- ... chromosomal 5q31.1 gain involving PITX1 causes Liebenberg syndrome. Am J Med Genet ... PN, Ibrahim DM, Franke M, Hecht J, Lohan S, Dathe K, Nardone AM, Ferrari ...
- ... family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome ... PA, Shaw GM, Hecht JT. The population-based prevalence of achondroplasia and ...
- ... doi: 10.4238/vol10-2gmr1111. Citation on PubMed Hecht JT, Makitie O, Hayes E, Haynes R, Susic ... Posey KL, Yang Y, Veerisetty AC, Sharan SK, Hecht JT. Model systems for studying skeletal dysplasias caused ...
- ... on PubMed or Free article on PubMed Central Hecht PJ, Lin TJ. Hallux valgus. Med Clin North ...
- ... on PubMed Lu J, Tiao G, Folkerth R, Hecht J, Walsh C, Sheen V. Overlapping expression of ...