176 related articles for article (PubMed ID: 1782201)
1. Congenital absence of all primary and permanent lateral incisors in a carrier of X-linked hypohidrotic ectodermal dysplasia.
McLaughlin WS
Int J Paediatr Dent; 1991 Aug; 1(2):99-103. PubMed ID: 1782201
[TBL] [Abstract][Full Text] [Related]
2. Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.
Crawford PJ; Aldred MJ; Clarke A
J Med Genet; 1991 Mar; 28(3):181-5. PubMed ID: 2051453
[TBL] [Abstract][Full Text] [Related]
3. Hypodontia and sweat pore counts in detecting carriers of X-linked hypohidrotic ectodermal dysplasia.
Sofaer JA
Br Dent J; 1981 Nov; 151(10):327-30. PubMed ID: 6946797
[No Abstract] [Full Text] [Related]
4. Hypohidrotic ectodermal dysplasia--a case report.
Gopinath VK; Manoj KM; Mahesh K
J Indian Soc Pedod Prev Dent; 1999 Sep; 17(3):90-2. PubMed ID: 10863497
[TBL] [Abstract][Full Text] [Related]
5. Hypohidrotic (anhidrotic) ectodermal dysplasia in female twins.
Ogunrinde GO; Zubair RO; Ajike SO; Ige SO
Niger J Clin Pract; 2012; 15(1):98-100. PubMed ID: 22437101
[TBL] [Abstract][Full Text] [Related]
6. Hypohidrotic ectodermal dysplasia: dental features and carriers detection.
Glavina D; Majstorović M; Lulić-Dukić O; Jurić H
Coll Antropol; 2001 Jun; 25(1):303-10. PubMed ID: 11787554
[TBL] [Abstract][Full Text] [Related]
7. X-linked recessive hypohidrotic ectodermal dysplasia. Manifestations and management.
Wright JT; Finley WH
Ala J Med Sci; 1986 Jan; 23(1):84-7. PubMed ID: 3953980
[No Abstract] [Full Text] [Related]
8. [Primary anodontia in X-linked hidrotic ectodermal dysplasia].
Beliakov IuA; Elizarova VM; Smirnova TA; Krotov VA
Stomatologiia (Mosk); 1998; 77(4):29-31. PubMed ID: 9752735
[TBL] [Abstract][Full Text] [Related]
9. Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygote.
Passarge E; Fries E
Birth Defects Orig Artic Ser; 1977; 13(3C):95-100. PubMed ID: 890117
[TBL] [Abstract][Full Text] [Related]
10. A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.
Nakata M; Koshiba H; Eto K; Nance WE
Am J Hum Genet; 1980 Nov; 32(6):908-19. PubMed ID: 7446529
[TBL] [Abstract][Full Text] [Related]
11. Hypohidrotic ectodermal dysplasia: argument against an autosomal recessive form clinically indistinguishable from X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome).
Sybert VP
Pediatr Dermatol; 1989 Jun; 6(2):76-81. PubMed ID: 2748478
[TBL] [Abstract][Full Text] [Related]
12. Anodontia with hypohidrotic ectodermal dysplasia in a young female: a case report.
Ohno K; Ohmori I
Pediatr Dent; 2000; 22(1):49-52. PubMed ID: 10730287
[TBL] [Abstract][Full Text] [Related]
13. A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia.
Spfaer JA
J Med Genet; 1981 Dec; 18(6):459-60. PubMed ID: 7334506
[TBL] [Abstract][Full Text] [Related]
14. [Syndromes 17. Hypohidrotic ectodermal dysplasia].
Baart JA; van Hagen JM
Ned Tijdschr Tandheelkd; 2000 Jan; 107(1):12-4. PubMed ID: 12621820
[TBL] [Abstract][Full Text] [Related]
15. Hereditary ectodermal dysplasia: a case report.
Suprabha BS
J Indian Soc Pedod Prev Dent; 2002 Mar; 20(1):37-40. PubMed ID: 12435032
[TBL] [Abstract][Full Text] [Related]
16. Hypohidrotic ectodermal dysplasia: a clinical case with a longitudinal approach.
Fraiz FC; Gugisch RC; Cavalcante-Leão BL; Macedo LM
J Contemp Dent Pract; 2014 Nov; 15(6):788-91. PubMed ID: 25825110
[TBL] [Abstract][Full Text] [Related]
17. X-linked hypohidrotic ectodermal dysplasia--an unusual prosthetic problem.
Nortjé CJ; Farman AG; Thomas CJ; Watermeyer GJ
J Prosthet Dent; 1978 Aug; 40(2):137-42. PubMed ID: 278831
[No Abstract] [Full Text] [Related]
18. [Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?].
Le Marec B; Roussey M; Chevrant-Breton J; Segalen J; Bourdinière J; Sénécal J
J Genet Hum; 1983 Dec; 31(4):279-93. PubMed ID: 6663288
[TBL] [Abstract][Full Text] [Related]
19. Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia.
Goodship J; Malcolm S; Clarke A; Pembrey ME
J Med Genet; 1990 Jul; 27(7):422-5. PubMed ID: 2395159
[TBL] [Abstract][Full Text] [Related]
20. A new autosomal dominant syndrome of hypohidrotic ectodermal dysplasia and unusual facies.
Bocian M; Rimoin DL
Birth Defects Orig Artic Ser; 1979; 15(5B):239-51. PubMed ID: 526580
[No Abstract] [Full Text] [Related]
[Next] [New Search]