126 related articles for article (PubMed ID: 3608221)
1. Trichodysplasia-xeroderma: an autosomal dominant condition.
Pinheiro M; Freire-Maia N
Clin Genet; 1987 May; 31(5):337-42. PubMed ID: 3608221
[TBL] [Abstract][Full Text] [Related]
2. Trichodermodysplasia with dental alterations: an apparently new genetic ectodermal dysplasia of the tricho-odonto-onychial subgroup.
Pinheiro M; Freire-Maia DV; Miranda E; Silva-Filho OG; Freire-Maia N
Clin Genet; 1986 Apr; 29(4):332-6. PubMed ID: 3720011
[TBL] [Abstract][Full Text] [Related]
3. Dermoodontodysplasia: an eleven-member, four generation pedigree with an apparently hitherto undescribed pure ectodermal dysplasia.
Pinheiro M; Freire-Maia N
Clin Genet; 1983 Jul; 24(1):58-68. PubMed ID: 6616948
[TBL] [Abstract][Full Text] [Related]
4. Family with autosomal dominant hidrotic ectodermal dysplasia: a previously unrecognised syndrome?
Christianson AL; Fourie S
Am J Med Genet; 1996 Jun; 63(4):549-53. PubMed ID: 8826433
[TBL] [Abstract][Full Text] [Related]
5. A distinct type of hidrotic ectodermal dysplasia.
Halal F; Setton N; Wang NS
Am J Med Genet; 1991 Mar; 38(4):552-6. PubMed ID: 2063897
[TBL] [Abstract][Full Text] [Related]
6. Autosomal dominant ectodermal dysplasia.
Jorgenson RJ; Dowben JS; Dowben SL
J Craniofac Genet Dev Biol; 1987; 7(4):403-12. PubMed ID: 3429615
[TBL] [Abstract][Full Text] [Related]
7. Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia.
Calzavara-Pinton P; Carlino A; Benetti A; De Panfilis G
Dermatologica; 1991; 182(3):184-7. PubMed ID: 1879585
[TBL] [Abstract][Full Text] [Related]
8. A newly recognized autosomal dominant ectodermal dysplasia syndrome: the odonto-tricho-ungual-digital-palmar syndrome.
Mendoza HR; Valiente MD
Am J Med Genet; 1997 Aug; 71(2):144-9. PubMed ID: 9217212
[TBL] [Abstract][Full Text] [Related]
9. Ectodermal dysplasia with corkscrew hairs: observation of probable autosomal dominant tricho-odonto-onychodysplasia with syndactyly.
Trüeb R; Burg G; Bottani A; Schinzel A
J Am Acad Dermatol; 1994 Feb; 30(2 Pt 1):289-90. PubMed ID: 8141890
[No Abstract] [Full Text] [Related]
10. Rapp-Hodgkin syndrome: report of a Brazilian family.
Rodini EO; Freitas JA; Richieri-Costa A
Am J Med Genet; 1990 Aug; 36(4):463-6. PubMed ID: 2389804
[TBL] [Abstract][Full Text] [Related]
11. Reevaluation of ichthyosis and hair shaft abnormalities.
Hurwitz S; Kirsch N; McGuire J
Arch Dermatol; 1971 Mar; 103(3):266-71. PubMed ID: 5107872
[No Abstract] [Full Text] [Related]
12. [Hidrotic form of ectodermal dysplasia].
Bolck F; Barth C
Z Hautkr; 1973 Dec; 48(24):1041-8. PubMed ID: 4273177
[No Abstract] [Full Text] [Related]
13. Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation: a possible "new" form of ectodermal dysplasia.
Winter RM; MacDermot KD; Hill FJ
Am J Med Genet; 1988 Jan; 29(1):209-16. PubMed ID: 3344769
[TBL] [Abstract][Full Text] [Related]
14. Concurrent hypohidrotic ectodermal dysplasia and X-linked ichthyosis.
Esterly NB; Pashayan HM; West CE
Am J Dis Child; 1973 Oct; 126(4):539-43. PubMed ID: 4544634
[No Abstract] [Full Text] [Related]
15. Hair-nail dysplasia--a new pure autosomal dominant ectodermal dysplasia.
Pinheiro M; Freire-Maia N
Clin Genet; 1992 Jun; 41(6):296-8. PubMed ID: 1623625
[TBL] [Abstract][Full Text] [Related]
16. On the genetics of hypodontia and microdontia: synergism or allelism of major genes in a family with six affected members.
Lyngstadaas SP; Nordbo H; Gedde-Dahl T; Thrane PS
J Med Genet; 1996 Feb; 33(2):137-42. PubMed ID: 8929951
[TBL] [Abstract][Full Text] [Related]
17. Properties of hair keratin in an autosomal dominant form of ectodermal dysplasia.
Gold RJ; Scriver CR
Am J Hum Genet; 1972 Sep; 24(5):549-61. PubMed ID: 5054225
[No Abstract] [Full Text] [Related]
18. The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.
Reynold JM; Gold MB; Scriver CR
Birth Defects Orig Artic Ser; 1971 Jun; 7(8):91-5. PubMed ID: 5173317
[TBL] [Abstract][Full Text] [Related]
19. Woolly hair--study of a family.
Verbov J
Dermatologica; 1978; 157(1):42-7. PubMed ID: 668970
[TBL] [Abstract][Full Text] [Related]
20. Rapp-Hodgkin hypohidrotic ectodermal dysplasia syndrome.
Walpole IR; Goldblatt J
Clin Genet; 1991 Feb; 39(2):114-20. PubMed ID: 2015692
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]