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25. Mutations in the lysyl hydroxylase 1 gene that result in enzyme deficiency and the clinical phenotype of Ehlers-Danlos syndrome type VI. Yeowell HN; Walker LC Mol Genet Metab; 2000; 71(1-2):212-24. PubMed ID: 11001813 [TBL] [Abstract][Full Text] [Related]
27. [Hereditary deficiency in the enzymes of the biosynthesis of collagen. The Ehlers-Danlos syndromes (author's transl)]. Gajdos A Nouv Presse Med; 1977 Oct; 6(34):3101-5. PubMed ID: 21384 [TBL] [Abstract][Full Text] [Related]
28. Nevo syndrome is allelic to the kyphoscoliotic type of the Ehlers-Danlos syndrome (EDS VIA). Giunta C; Randolph A; Al-Gazali LI; Brunner HG; Kraenzlin ME; Steinmann B Am J Med Genet A; 2005 Mar; 133A(2):158-64. PubMed ID: 15666309 [TBL] [Abstract][Full Text] [Related]
29. The Ehlers-Danlos syndromes. Yeowell HN; Pinnell SR Semin Dermatol; 1993 Sep; 12(3):229-40. PubMed ID: 8217561 [TBL] [Abstract][Full Text] [Related]