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22. [CHILD syndrome. Case report of a rare genetic dermatosis]. Peter C; Meinecke P Hautarzt; 1993 Sep; 44(9):590-3. PubMed ID: 8407327 [TBL] [Abstract][Full Text] [Related]
23. Pathological findings in one of two siblings with Sjögren-Larsson Syndrome. Silva CA; Saraiva A; Gonçalves V; de Sousa G; Martins R; Cruz C Eur Neurol; 1980; 19(3):166-70. PubMed ID: 7389762 [TBL] [Abstract][Full Text] [Related]
24. [You make the diagnosis. Neurocutaneous dysplasia: Sjögren-Larsson syndrome]. Elliott P; Schober E; Frisch H Padiatr Padol; 1989; 24(2):149-52. PubMed ID: 2762000 [No Abstract] [Full Text] [Related]
26. Sjögren-Larsson syndrome: microscopic and scanning electron microscopic findings in replicas of the skin. Jagell S; Hofer PA Acta Derm Venereol; 1982; 62(5):397-400. PubMed ID: 6183888 [TBL] [Abstract][Full Text] [Related]
27. [Genetic counseling in Sjögren-Larsson syndrome (author's transl)]. Theile U Z Orthop Ihre Grenzgeb; 1978; 116(6):912-4. PubMed ID: 726579 [TBL] [Abstract][Full Text] [Related]
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35. [Atypical erythrokeratodermia with deafness, keratitis and double mycotic infection]. Ginter G; Soyer HP Z Hautkr; 1988 Nov; 63(11):951-7. PubMed ID: 3239140 [TBL] [Abstract][Full Text] [Related]
36. Next-generation sequencing through multi-gene panel testing for diagnosis of hereditary ichthyosis in Chinese. Cheng R; Liang J; Li Y; Zhang J; Ni C; Yu H; Kong X; Li M; Yao Z Clin Genet; 2020 May; 97(5):770-778. PubMed ID: 31953843 [TBL] [Abstract][Full Text] [Related]
37. Report of a family with an unusual expression of recessive ichthyosis. Review of 42 cases. Bernhardt M; Baden HP Arch Dermatol; 1986 Apr; 122(4):428-33. PubMed ID: 3954411 [TBL] [Abstract][Full Text] [Related]
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