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2. [Case of craniometaphyseal dysplasia with deformity of the face and optic nerve atrophy in siblings]. Yamanaka T; Sakuma Y; Ando M Ganka; 1970 Dec; 12(12):1012-7. PubMed ID: 5530819 [No Abstract] [Full Text] [Related]
5. [Clinical evolution and chromosome study of a case of Albright's syndrome]. Cerruti Mainardi P; Arena GC; Grasso M Minerva Pediatr; 1967 Mar; 19(11):487-94. PubMed ID: 4304967 [No Abstract] [Full Text] [Related]
7. [A case of craniometaphyseal dysplasia]. Kojima K; Niimi K; Tamaki M Nippon Ganka Gakkai Zasshi; 1967 Jun; 71(6):698-702. PubMed ID: 5624657 [No Abstract] [Full Text] [Related]
8. Craniometaphyseal dysplasia: the first successful surgical treatment for associated hearing loss. Shea J; Gerbe R; Ayani N Laryngoscope; 1981 Aug; 91(8):1369-74. PubMed ID: 7266214 [No Abstract] [Full Text] [Related]
9. Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. I. Familial metaphyseal dysplasia and craniometaphyseal dysplasia; their relation to leontiasis ossea and osteopetrosis; disorders of bone remodeling. JACKSON WP; ALBRIGHT F; DREWRY G; HANELIN J; RUBIN MI AMA Arch Intern Med; 1954 Dec; 94(6):871-85. PubMed ID: 13217486 [No Abstract] [Full Text] [Related]
10. [Atypical familial condensing osteosis with leontiasis ossea]. Jouve P; Bernard R; Giraud F; Debaene A J Radiol Electrol Med Nucl; 1970 Nov; 51(11):699-704. PubMed ID: 5489118 [No Abstract] [Full Text] [Related]
11. A whistling face syndrome case with bilateral skin dimples. Buyukavci M; Tan H; Eren S; Balci S Genet Couns; 2005; 16(1):71-3. PubMed ID: 15844782 [TBL] [Abstract][Full Text] [Related]
13. Osteoglophonic dysplasia: review and further delineation of the syndrome. Sklower Brooks S; Kassner G; Qazi Q; Keogh MJ; Gorlin RJ Am J Med Genet; 1996 Dec; 66(2):154-62. PubMed ID: 8958322 [TBL] [Abstract][Full Text] [Related]
14. Correction of maxillary retrognathia in a case of craniometaphyseal dysplasia. Laurian N; Zohar Y J Oral Surg; 1980 Aug; 38(8):609-12. PubMed ID: 6930464 [TBL] [Abstract][Full Text] [Related]
15. [Family affected by hyperostosis frontalis interna (Morgagni-Morel syndrome) through 4 successive generations]. Rosatti P J Genet Hum; 1972 Sep; 20(3):207-52. PubMed ID: 4659165 [No Abstract] [Full Text] [Related]
16. Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr-381 residue in FGFR2 gene. Collet C; Alessandri JL; Arnaud E; Balu M; Daire VC; Di Rocco F Clin Genet; 2014 Jun; 85(6):598-9. PubMed ID: 23808569 [No Abstract] [Full Text] [Related]
17. Craniometaphyseal dysplasia: case report. Maia LC; Modesto A; Carakushansky G; de Souza IP Braz Dent J; 2000; 11(2):153-60. PubMed ID: 11210264 [TBL] [Abstract][Full Text] [Related]
18. The question of hypertelorism in oculodentoosseous dysplasia. Fará M; Gorlin RJ Am J Med Genet; 1981; 10(1):101-2. PubMed ID: 6794368 [No Abstract] [Full Text] [Related]