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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
191 related items for PubMed ID: 6808331
41. Surgical management of the hand in Freeman-Sheldon syndrome. Kalliainen LK, Drake DB, Edgerton MT, Grzeskiewicz JL, Morgan RF. Ann Plast Surg; 2003 May; 50(5):456-62; discussion 463-70. PubMed ID: 12792532 [Abstract] [Full Text] [Related]
42. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. Feingold M, Hall BD, Lacassie Y, Martínez-Frías ML. Am J Med Genet; 1997 Mar 31; 69(3):245-9. PubMed ID: 9096752 [Abstract] [Full Text] [Related]
43. [Low cholesterol and pathological manifestations: Smith-Lemli-Opitz syndrome]. Franceschini P, Franceschini D. Minerva Pediatr; 1994 Dec 31; 46(12):579-80. PubMed ID: 7731422 [No Abstract] [Full Text] [Related]
44. Megalocornea-mental retardation syndrome: an additional case. Antiñolo G, Rufo M, Borrego S, Morales C. Am J Med Genet; 1994 Aug 15; 52(2):196-7. PubMed ID: 7802008 [Abstract] [Full Text] [Related]
45. Ocular hypertelorism and nasal agenesis (midface syndrome) with limb anomalies. Calli LJ. Birth Defects Orig Artic Ser; 1971 Jun 15; 7(7):268. PubMed ID: 5173220 [No Abstract] [Full Text] [Related]
46. Lujan-Fryns syndrome in the differential diagnosis of schizophrenia. De Hert M, Steemans D, Theys P, Fryns JP, Peuskens J. Am J Med Genet; 1996 Apr 09; 67(2):212-4. PubMed ID: 8723050 [Abstract] [Full Text] [Related]
47. [Whistling face syndrome (Burian)]. Rickhey B. Z Orthop Ihre Grenzgeb; 1971 Jul 09; 109(3):532-4. PubMed ID: 4254815 [No Abstract] [Full Text] [Related]
48. 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 09; 15(9):790-2. PubMed ID: 16101713 [Abstract] [Full Text] [Related]
51. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis. Terespolsky D, Farrell SA, Siegel-Bartelt J, Weksberg R. Am J Med Genet; 1995 Nov 20; 59(3):329-33. PubMed ID: 8599356 [Abstract] [Full Text] [Related]
56. New syndrome of macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay. Bagatelle R, Cassidy SB. Am J Med Genet; 1995 Jan 30; 55(3):367-71. PubMed ID: 7537019 [Abstract] [Full Text] [Related]
57. Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children. Galán-Gómez E, Cardesa-García JJ, Campo-Sampedro FM, Salamanca-Maesso C, Martínez-Frías ML, Frías JL. Am J Med Genet; 1995 Nov 20; 59(3):276-82. PubMed ID: 8599349 [Abstract] [Full Text] [Related]