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2. [Report of a case of Goltz-Gorlin syndrome]. Rodermund OE; Hausmann D Hautarzt; 1977 Jan; 28(1):37-9. PubMed ID: 190190 [TBL] [Abstract][Full Text] [Related]
3. Odontoonychodysplasia with alopecia: a new pure ectodermal dysplasia with probable autosomal recessive inheritance. Pinheiro M; Freire-Maia N; Gollop TR Am J Med Genet; 1985 Jan; 20(1):197-202. PubMed ID: 2982262 [TBL] [Abstract][Full Text] [Related]
4. A case of cardio-facio-cutaneous syndrome. Mucklow ES Am J Med Genet; 1989 Aug; 33(4):474-5. PubMed ID: 2596506 [TBL] [Abstract][Full Text] [Related]
7. [Relationship between aplasia cutis congenita circumscripta and Goltz's syndrome]. Arpád F; József M; László S Orv Hetil; 1975 May; 116(21):1227-30. PubMed ID: 1173281 [No Abstract] [Full Text] [Related]
9. Cardio-facio-cutaneous (CFC) syndrome in a child carrying an inherited inversion of chromosome 7. Lopez-Rangel E; Hrynchak M; Friedman JM Am J Med Genet; 1993 Sep; 47(3):326-9. PubMed ID: 8135275 [TBL] [Abstract][Full Text] [Related]
10. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia. Fadhil M; Ghabra TA; Deeb M; Der Kaloustian VM Am J Med Genet; 1983 Feb; 14(2):335-46. PubMed ID: 6837628 [TBL] [Abstract][Full Text] [Related]
11. Ectodermal dysplasia syndrome with eyebrow alopecia, ptosis, strabismus, nystagmus, joint laxity, cerebellar ataxia, and osteopenia. Zannolli R; Inchingolo G; Serracca L; Miracco C; De Santi MM; Malandrini A; Biagioli M; Perotti R; Baldi C; Nuti D; Polito E; Gonnelli S Am J Med Genet; 2002 Nov; 113(1):111-3. PubMed ID: 12400077 [No Abstract] [Full Text] [Related]
12. [FAMILIAL ECTODERMAL DYSPLASIA OF THE HIDROTIC TYPE]. MALLMANN-MUEHLBERGER E; HELWIG H Ann Paediatr; 1964; 202():358-70. PubMed ID: 14168318 [No Abstract] [Full Text] [Related]
17. [Goltz' syndrome. Bone, eye and skin dysplasias]. Fazekas A; Szegö L; Vigváry L; Nagy M Z Haut Geschlechtskr; 1973 Apr; 48(8):307-15. PubMed ID: 4708606 [No Abstract] [Full Text] [Related]
18. A new case of Balci's syndrome (corneal opacity, microphthalmia, microcephaly, mental retardation, and generalized muscular spasticity associated with congenital heart disease). Balci S; Demirçeken FG; Ocal B; Zorlu P; Teziç T Turk J Pediatr; 2001; 43(4):366-8. PubMed ID: 11765173 [TBL] [Abstract][Full Text] [Related]
19. A suggested mode of pigment transfer into the dermis. Guerrier C Acta Derm Venereol; 1973; 53(3):173-7. PubMed ID: 4124006 [No Abstract] [Full Text] [Related]
20. [Polydysplasia with dermal hypoplasia in some areas]. Stewart WM; Lauret P; Michel Y Bull Soc Fr Dermatol Syphiligr; 1969; 76(6):812-4. PubMed ID: 5396013 [No Abstract] [Full Text] [Related] [Next] [New Search]