These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
142 related items for PubMed ID: 7793794
1. Familial Saethre-Chotzen syndrome with or without polydactyly of the toe. Shidayama R, Hirano A, Iio Y, Fujii T. Ann Plast Surg; 1995 Apr; 34(4):435-40. PubMed ID: 7793794 [Abstract] [Full Text] [Related]
2. The Saethre-Chotzen syndrome with partial bifid of the distal phalanges of the great toes. Observations of three cases in one family. Kopyść Z, Stańska M, Ryzko J, Kulczyk B. Hum Genet; 1980 Apr; 56(2):195-204. PubMed ID: 7450776 [Abstract] [Full Text] [Related]
3. Saethre-Chotzen syndrome: a broad and variable pattern of skeletal malformations. Friedman JM, Hanson JW, Graham CB, Smith DW. J Pediatr; 1977 Dec; 91(6):929-23. PubMed ID: 925822 [Abstract] [Full Text] [Related]
5. A novel mutation in the TWIST gene, implicated in Saethre-Chotzen syndrome, is found in the original case of Robinow-Sorauf syndrome. Cai J, Shoo BA, Sorauf T, Jabs EW. Clin Genet; 2003 Jul; 64(1):79-82. PubMed ID: 12791045 [No Abstract] [Full Text] [Related]
9. A family with the Saethre-Chotzen syndrome. Bianchi E, Aricŏ M, Podestă AF, Grana M, Fiori P, Beluffi G. Am J Med Genet; 1985 Dec; 22(4):649-58. PubMed ID: 4073118 [Abstract] [Full Text] [Related]
11. Cephalic malformations in Saethre-Chotzen syndrome. Acrocephalosyndactyly type III. Evans CA, Christiansen RL. Radiology; 1976 Nov; 121(2):399-403. PubMed ID: 981618 [Abstract] [Full Text] [Related]
12. Identification of a frameshift mutation in the gene TWIST in a family affected with Robinow-Sorauf syndrome. Kunz J, Hudler M, Fritz B. J Med Genet; 1999 Aug; 36(8):650-2. PubMed ID: 10465122 [No Abstract] [Full Text] [Related]
13. A novel frameshift mutation of the GLI3 gene in a family with broad thumbs with/without big toes, postaxial polydactyly and variable syndactyly of the hands/feet. Al-Qattan MM. Clin Genet; 2012 Nov; 82(5):502-4. PubMed ID: 22428873 [No Abstract] [Full Text] [Related]
14. Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly. Assadsangabi R, Hajmomenian M, Bilaniuk LT, Vossough A. Childs Nerv Syst; 2015 May; 31(5):735-41. PubMed ID: 25686894 [Abstract] [Full Text] [Related]
15. A child with Saethre-Chotzen syndrome, sensorineural hearing loss, and a TWIST mutation. Lee S, Seto M, Sie K, Cunningham M. Cleft Palate Craniofac J; 2002 Jan; 39(1):110-4. PubMed ID: 11772178 [Abstract] [Full Text] [Related]
16. Atypical crossed polydactyly in two siblings with Ellis-van Creveld Syndrome and mild clinical manifestations in close relatives. Okten A, Cakir M, Orhan F, Mungan I. Pediatr Int; 2004 Apr; 46(2):184-7. PubMed ID: 15056248 [No Abstract] [Full Text] [Related]