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67. Conradi-Hünermann disease. Case report and mini-review. Paltzik RL; Ente G; Penzer PH; Goldblum LM Cutis; 1982 Feb; 29(2):174-180. PubMed ID: 7060406 [No Abstract] [Full Text] [Related]
68. [Description of chondrodysplasia calcificans congenita and its relation to chondrodysplasia foetalis]. SCHONENBERG H; SCHALLOCK G Ann Paediatr; 1953 Mar; 180(3):129-62. PubMed ID: 13058210 [No Abstract] [Full Text] [Related]
69. [The clinical picture of chondrodysplasia calcificans congenita]. Lyrakos A; Richter J Z Orthop Ihre Grenzgeb; 1969 May; 106(2):379-93. PubMed ID: 4240699 [No Abstract] [Full Text] [Related]
70. [Hip joint sonography in skeletal dysplasias with metaphyseal involvement. Possibilities of erroneous assessments]. Schumacher R; Leicher-Düber A; Pontz BF Rofo; 1988 Oct; 149(4):414-6. PubMed ID: 2845511 [TBL] [Abstract][Full Text] [Related]
71. [CONTRIBUTION TO THE CLINICAL PICTURE OF CHONDRODYSTROPHIA CALCIFICANS CONGENITA (CONRADI-HUENERMANN)]. MAYER H; WOLLENSAK J; DAMEROW R Z Kinderheilkd; 1964 Nov; 91():282-96. PubMed ID: 14333491 [No Abstract] [Full Text] [Related]
72. Upington disease: a familial dyschondroplasia. Schweitzer G; Jones B; Timme A S Afr Med J; 1971 Sep; 45(36):994-1000. PubMed ID: 5316541 [No Abstract] [Full Text] [Related]
73. Dysplasia epiphysialis hemimelica (epiphyseal osteochondromata). Report of two cases and review of the literature. Theodorou S; Lanitis G Helv Paediatr Acta; 1968 Apr; 23(2):195-204. PubMed ID: 4881354 [No Abstract] [Full Text] [Related]
75. Case of Conradi-Hünermann-Happle syndrome due to a nonsense mutation of c.245G>A (p.W82*). Satake M; Kudo K; Sasaki T; Furue M; Kubo A J Dermatol; 2019 Aug; 46(8):e296-e298. PubMed ID: 30809841 [No Abstract] [Full Text] [Related]
76. Diagnosis and counselling in Conradi disease. Merchant RH; Shah KN; Mehta KP; Desai MP; Patkar SL; Ambani L Indian J Pediatr; 1982; 49(400):767-9. PubMed ID: 7188201 [No Abstract] [Full Text] [Related]
77. Non-lethal non-mosaic male with Conradi-Hunermann syndrome caused by a novel EBP c.356T>G mutation. Bode H; Galm C; Hummler H; Teller C; Haas D; Gencik M Am J Med Genet A; 2013 Sep; 161A(9):2385-8. PubMed ID: 23852825 [No Abstract] [Full Text] [Related]
78. [A contribution to the disease pattern of osteolysis (author's transl)]. Schalwig J Z Orthop Ihre Grenzgeb; 1981 Oct; 119(5):481-5. PubMed ID: 7314820 [TBL] [Abstract][Full Text] [Related]
79. [Unilateral enchondromatosis with multiple lymphangiokeratomas. Nosology of Maffucci's syndrome]. Raff M; Wickenhauser J Hautarzt; 1973 Jul; 24(7):309-13. PubMed ID: 4724783 [No Abstract] [Full Text] [Related]
80. [Chondrodysplasia punctata (author's transl)]. Kost M; Gadomska L; Weseli R Pol Przegl Radiol Med Nukl; 1977; 41(5):339-43. PubMed ID: 604955 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]