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Journal Abstract Search
163 related items for PubMed ID: 3789012
1. New evidence for genetic heterogeneity of the Freeman-Sheldon syndrome. Sánchez JM, Kaminker CP. Am J Med Genet; 1986 Nov; 25(3):507-11. PubMed ID: 3789012 [Abstract] [Full Text] [Related]
2. Further evidence for genetic heterogeneity of whistling face or Freeman-Sheldon syndrome in a Chinese family. Wang TR, Lin SJ. Am J Med Genet; 1987 Oct; 28(2):471-5. PubMed ID: 3425620 [Abstract] [Full Text] [Related]
3. [Cranio-carpo-tarsal dysplasia syndrome (Freeman-Sheldon syndrome, whistling face syndrome)]. Träger D. Z Orthop Ihre Grenzgeb; 1987 Oct; 125(1):106-7. PubMed ID: 3577337 [Abstract] [Full Text] [Related]
4. Whistling face (Freeman-Sheldon) syndrome in two siblings. Bekir N, Bayraktaroğlu Z, Coşkun Y, Karaaslan C. Turk J Pediatr; 1994 Oct; 36(4):329-32. PubMed ID: 7825240 [Abstract] [Full Text] [Related]
5. Freeman-Sheldon syndrome. A case report and review of the literature. Ferrari D, Bettuzzi C, Donzelli O. Chir Organi Mov; 2008 Sep; 92(2):127-31. PubMed ID: 18677448 [Abstract] [Full Text] [Related]
6. A whistling face syndrome case with bilateral skin dimples. Buyukavci M, Tan H, Eren S, Balci S. Genet Couns; 2005 Sep; 16(1):71-3. PubMed ID: 15844782 [Abstract] [Full Text] [Related]
9. Long term follow-up of two sibs with an autosomal recessive form of chrondrodysplasia punctata and epilepsy. Stoll C, Pauly F, Steib JP. Genet Couns; 2004 Sep; 15(4):411-20. PubMed ID: 15658616 [Abstract] [Full Text] [Related]
10. Freeman-Sheldon syndrome: a case report. Aren G, Yurdabakan Z, Ozcan I. Quintessence Int; 2003 Apr; 34(4):307-10. PubMed ID: 12731619 [Abstract] [Full Text] [Related]
11. Gellis SS, Feingold M: Picture of the month: Crano-carpo-tarsal dystrophy. (Whistling face syndrome, Freeman-Sheldon Syndrome). Am J Dis Child; 1970 Apr; 119(4):339-40. PubMed ID: 5434592 [No Abstract] [Full Text] [Related]
13. [A rare hand malformation, the Freeman-Sheldon syndrome]. Freilinger G, Rett A, Killian W. Handchirurgie; 1980 Jun 23; 12(3-4):225-7. PubMed ID: 7333533 [Abstract] [Full Text] [Related]
14. Autosomal dominant inheritance in Setleis syndrome. Masuno M, Imaizumi K, Makita Y, Nakamura M, Kuroki Y. Am J Med Genet; 1995 May 22; 57(1):57-60. PubMed ID: 7645599 [Abstract] [Full Text] [Related]
15. Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneity. Schrander-Stumpel C, Fryns JP, Beemer FA, Rive FA. Am J Med Genet; 1991 Mar 15; 38(4):557-61. PubMed ID: 2063898 [Abstract] [Full Text] [Related]
16. M--craniocarpotarsal dystrophy (whistling face syndrome) in two families. Jorgenson RJ. Birth Defects Orig Artic Ser; 1974 Mar 15; 10(5):237-42. PubMed ID: 4220006 [No Abstract] [Full Text] [Related]
17. Genetic heterogeneity in the Freeman-Sheldon syndrome: two adults with probable autosomal recessive inheritance. Fitzsimmons JS, Zaldua V, Chrispin AR. J Med Genet; 1984 Oct 15; 21(5):364-8. PubMed ID: 6502650 [Abstract] [Full Text] [Related]
18. Awake nasotracheal intubation using fiberoptic bronchoscope in a pediatric patient with Freeman-Sheldon syndrome. Kim JS, Park SY, Min SK, Kim JH, Lee SY, Moon BK. Paediatr Anaesth; 2005 Sep 15; 15(9):790-2. PubMed ID: 16101713 [Abstract] [Full Text] [Related]
20. [Anesthetic management of an infant with Freeman-Sheldon syndrome]. Okawa M, Kinouchi K, Kitamura S, Taniguchi A, Sasaoka N, Fukumitsu K. Masui; 2002 Jun 15; 51(6):659-62. PubMed ID: 12134659 [Abstract] [Full Text] [Related] Page: [Next] [New Search]