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3. [Peculiarities and dynamics of changes in the foci of multiple epiphyseal dysplasia (Fairbank's disease) in combination with epiphyseal fractures]. Koval' MA Vestn Rentgenol Radiol; 1967; 12(3):83-6. PubMed ID: 5614455 [No Abstract] [Full Text] [Related]
4. The genetics of follicular atrophoderma. Curth HO Arch Dermatol; 1978 Oct; 114(10):1479-83. PubMed ID: 718183 [TBL] [Abstract][Full Text] [Related]
5. Acute skin manifestations of Conradi-Huenermann syndrome in a male adult. Crovato F; Rebora A Arch Dermatol; 1985 Aug; 121(8):1064-5. PubMed ID: 4026347 [TBL] [Abstract][Full Text] [Related]
9. [A case of multiple exostotic chondrodysplasia in combination with Wolf-Parkinson-White syndrome]. Morova NA; Ignat'ev IuT; Chetverikov SIu; Stefanenko GN Klin Med (Mosk); 2002; 80(8):64-5. PubMed ID: 12360625 [TBL] [Abstract][Full Text] [Related]
10. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome. Toriello HV; Higgins JV; Miller T Am J Med Genet; 1993 Oct; 47(5):797-9. PubMed ID: 8267015 [TBL] [Abstract][Full Text] [Related]
11. Vitreoretinal abnormalities in the Conradi-Hunermann form of chondrodysplasia punctata. Ramkissoon YD; Mayer EJ; Gibbon C; Haynes RJ Br J Ophthalmol; 2004 Jul; 88(7):973-4. PubMed ID: 15205255 [No Abstract] [Full Text] [Related]
12. Osteoarthrosis of the hip joints in multiple epiphyseal dysplasia. Emr J; Marecek V Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1974; 17(5):473-9. PubMed ID: 4534821 [No Abstract] [Full Text] [Related]
13. Osebold-Remondini syndrome vs chondrodysplasia punctata. Sheffield LJ; Mayne VM; Danks DM Am J Med Genet; 1987 Oct; 28(2):507, 509. PubMed ID: 3425625 [No Abstract] [Full Text] [Related]
14. X-linked dominant chondrodysplasia punctata/ichthyosis/cataract syndrome in males. Happle R Am J Med Genet; 1995 Jul; 57(3):493. PubMed ID: 7677158 [No Abstract] [Full Text] [Related]
16. XXY male with X-linked dominant chondrodysplasia punctata (Happle syndrome). Sutphen R; Amar MJ; Kousseff BG; Toomey KE Am J Med Genet; 1995 Jul; 57(3):489-92. PubMed ID: 7677157 [TBL] [Abstract][Full Text] [Related]
17. Cervical spinal cord compression in chondrodysplasia punctata. Case illustration. Yang BP; Mindea SA; DiPatri AJ J Neurosurg; 2006 Mar; 104(3 Suppl):212. PubMed ID: 16572643 [No Abstract] [Full Text] [Related]
18. 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; 15(4):411-20. PubMed ID: 15658616 [TBL] [Abstract][Full Text] [Related]
19. Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism. Traupe H; Vetter U; Happle R; Fisher LW; Cremers FP; Landy SJ; Pankau R; Ropers HH Hum Genet; 1993 Mar; 91(1):89-90. PubMed ID: 8454295 [No Abstract] [Full Text] [Related]
20. [The congenital disease of stippled epiphyses and its ophthalmologic manifestations]. Viallefont H; Costeau J Arch Ophtalmol Rev Gen Ophtalmol; 1969; 29(6):575-86. PubMed ID: 4242359 [No Abstract] [Full Text] [Related] [Next] [New Search]