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65. Focal dermal hypoplasia (Goltz syndrome): case reports. Derks B; Gericke GS; Louw M S Afr Med J; 1978 Jul; 54(1):27-9. PubMed ID: 211652 [TBL] [Abstract][Full Text] [Related]
66. Focal dermal hypoplasia. A nine-year follow-up study. Gottlieb SK; Fisher BK; Violin GA Arch Dermatol; 1973 Oct; 108(4):551-3. PubMed ID: 4745291 [No Abstract] [Full Text] [Related]
67. [Skull and tooth abnormalities in a patient with osteopathia striata]. De Boer SM; Van Gool AV Ned Tijdschr Geneeskd; 1974 Sep; 118(36):1373-80. PubMed ID: 4410894 [No Abstract] [Full Text] [Related]
68. Focal dermal hypoplasia syndrome. A review of the literature and report of two cases. Goltz RW; Henderson RR; Hitch JM; Ott JE Arch Dermatol; 1970 Jan; 101(1):1-11. PubMed ID: 5416790 [No Abstract] [Full Text] [Related]
70. [Chondrodysplastic nanism with congenital adrenal insufficiency and chronic lymphopenia. A new familial syndrome ((proceedings)]. Cret L; Bourgeois J; Souillet G; Thomas A; David M; Jeune M Pediatrie; 1976 Sep; 31(6):616-7. PubMed ID: 1005000 [No Abstract] [Full Text] [Related]
72. [Nanism with serious retardation of the skeletal maturation]. Campailla E; Martinelli B Clin Ortop; 1972; 23(1):50-3. PubMed ID: 5084894 [No Abstract] [Full Text] [Related]
73. Report of a case: acromesomelic dysplasia: radiologic, clinical, and pathological study. Fernández del Moral R; Santolaya Jiménez JM; Rodríguez González JI; Franco Vicario R Am J Med Genet; 1989 Jul; 33(3):415-9. PubMed ID: 2801778 [TBL] [Abstract][Full Text] [Related]
79. Osteopathia striata associated with familial dermopathy and white forelock: evidence for postnatal development of osteopathia striata. Whyte MP; Murphy WA Am J Med Genet; 1980; 5(3):227-34. PubMed ID: 7405956 [TBL] [Abstract][Full Text] [Related]
80. Focal dermal hypoplasia syndrome. The second known case in Japan. Yoshikawa K; Enami H; Takahashi A Arch Dermatol; 1978 Jul; 114(7):1078-9. PubMed ID: 686730 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]