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22. [Congenital cutis laxa. A case report with an electron microscopic study]. Sauviat C; Durepaire RM; Cesarini JP; Borde M Ann Pediatr (Paris); 1978 Sep; 25(7):355-61. PubMed ID: 16114347 [No Abstract] [Full Text] [Related]
23. The "Michelin tire baby syndrome": an autosomal dominant trait. Kunze J Am J Med Genet; 1986 Sep; 25(1):169-71. PubMed ID: 3799718 [No Abstract] [Full Text] [Related]
24. Cutis laxa. Brown FR; Holbrook KA; Byers PH; Stewart D; Dean J; Pyeritz RE Johns Hopkins Med J; 1982 Apr; 150(4):148-53. PubMed ID: 7062577 [No Abstract] [Full Text] [Related]
25. [Cutis laxa. Classification, clinical aspects and molecular defects]. Mensing H; Krieg T; Meigel W; Braun-Falco O Hautarzt; 1984 Oct; 35(10):506-11. PubMed ID: 6500933 [TBL] [Abstract][Full Text] [Related]
26. A case of Michelin tire baby syndrome with a thickened epiglottis. Samarin FM; Baum ED; Antaya RJ Pediatr Dermatol; 2010; 27(1):79-81. PubMed ID: 20199417 [TBL] [Abstract][Full Text] [Related]
27. The "Michelin tire baby" syndrome--an autosomal dominant trait. Niikawa N; Ishikiriyama S; Shikimani T Am J Med Genet; 1985 Nov; 22(3):637-8. PubMed ID: 4061498 [No Abstract] [Full Text] [Related]
28. [Congenital cutis laxa]. De Anda G; Vignale RA Med Cutan Ibero Lat Am; 1984; 12(1):1-5. PubMed ID: 6234443 [TBL] [Abstract][Full Text] [Related]
34. [Generalized Marfanoid congenital cutis laxa with lethal outcome: type V]. Larrègue M; Bonneau D; Boureau C; De Giacomoni P Ann Dermatol Venereol; 1990; 117(11):823-4. PubMed ID: 2099692 [No Abstract] [Full Text] [Related]
35. Gerodermia osteodysplastica/wrinkly skin syndrome: report of three patients and brief review of the literature. Nanda A; Alsaleh QA; Al-Sabah H; Marzouk EE; Salam AM; Nanda M; Anim JT Pediatr Dermatol; 2008; 25(1):66-71. PubMed ID: 18304158 [TBL] [Abstract][Full Text] [Related]
36. Congenital cutis laxa syndrome: type II autosomal recessive inheritance. Tüysüz B; Arapoğlu M; Ilikkan B; Demirkesen C; Perk Y Turk J Pediatr; 2003; 45(3):265-8. PubMed ID: 14696810 [TBL] [Abstract][Full Text] [Related]
37. Cutis laxa type II and wrinkly skin syndrome: distinct phenotypes. Gupta N; Phadke SR Pediatr Dermatol; 2006; 23(3):225-30. PubMed ID: 16780467 [TBL] [Abstract][Full Text] [Related]
38. Defective protein glycosylation in patients with cutis laxa syndrome. Morava E; Wopereis S; Coucke P; Gillessen-Kaesbach G; Voit T; Smeitink J; Wevers R; Grünewald S Eur J Hum Genet; 2005 Apr; 13(4):414-21. PubMed ID: 15657616 [TBL] [Abstract][Full Text] [Related]
39. [A case of cutis laxa with high stature]. Okada S; Mori M; Yamada M; Kogure M; Nagasawa T; Kobayashi S Nihon Naika Gakkai Zasshi; 1986 Apr; 75(4):576-81. PubMed ID: 3734548 [No Abstract] [Full Text] [Related]
40. Congenital cutis laxa: a case report and review of loose skin syndromes. Thomas WO; Moses MH; Craver RD; Galen WK Ann Plast Surg; 1993 Mar; 30(3):252-6. PubMed ID: 8494307 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]