230 related articles for article (PubMed ID: 6663288)
1. [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]
2. [Anhidrotic ectodermal dysplasia. Apropos of a case report of quadruplets].
Delaire J; Schmidt J; Lumineau JP; Pressard J; Billet J
Rev Stomatol Chir Maxillofac; 1984; 85(1):34-7. PubMed ID: 6584956
[TBL] [Abstract][Full Text] [Related]
3. [Anhidrotic ectodermal dysplasia. Clinico-genetic study of 4 families].
Balestrazzi P; Solli R; Salami P; Corrini L; Mattioli M; Bernasconi S
Minerva Pediatr; 1979 Feb; 31(4):265-74. PubMed ID: 460084
[No Abstract] [Full Text] [Related]
4. [Oligodontia in 2 siblings with ectodermal dysplasia].
Perzyna B; Anholcer H; Stolzmann W
Czas Stomatol; 1985 Jul; 38(7):492-8. PubMed ID: 3869903
[No Abstract] [Full Text] [Related]
5. Athelia in a female infant - heterozygous for anhidrotic ectodermal dysplasia.
Burck U; Held KR
Clin Genet; 1981 Feb; 19(2):117-21. PubMed ID: 7471507
[TBL] [Abstract][Full Text] [Related]
6. Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features.
Anton-Lamprecht I; Schleiermacher E; Wolf M
Birth Defects Orig Artic Ser; 1988; 24(2):183-95. PubMed ID: 3179426
[No Abstract] [Full Text] [Related]
7. Herediatary anhidrotic ectodermal dysplasia. Studies in a Nigerian famil.
Familusi JB; Jaiyesimi F; Ojo CO; Attah EB
Arch Dis Child; 1975 Aug; 50(8):642-7. PubMed ID: 1200681
[TBL] [Abstract][Full Text] [Related]
8. X-linked anhidrotic ectodermal dysplasia with some unusual features.
Settineri WM; Salzano FM; Fretas MJ
J Med Genet; 1976 Jun; 13(3):212-6. PubMed ID: 933122
[TBL] [Abstract][Full Text] [Related]
9. Three successive generations of women with anhidrotic/hypohidrotic ectodermal dysplasia.
Rodrigues RG
J Natl Med Assoc; 2005 Jan; 97(1):99-101. PubMed ID: 15719880
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Unusual physical features and heat stroke presentation for hypohydrotic ectodermal dysplasia.
Prasun P; Karmarkar SA; Agarwal A; W Stockton D
Clin Dysmorphol; 2012 Jan; 21(1):24-26. PubMed ID: 21959862
[TBL] [Abstract][Full Text] [Related]
12. [A case of anhidrotic ectodermal dysplasia in 3 brothers. Dental problems].
Moreau JL; Terrisse JP
Actual Odontostomatol (Paris); 1983 Sep; (143):469-77. PubMed ID: 6660086
[No Abstract] [Full Text] [Related]
13. Familial ectodermal dysplasia: a peers' agony.
Hegde K; Kashyap RR; Nair G; Nair PP
BMJ Case Rep; 2013 Jul; 2013():. PubMed ID: 23880572
[TBL] [Abstract][Full Text] [Related]
14. [Anhidrotic ectodermal dysplasia in a 56-year-old man and its complications].
Liashenko IN; Sokolov AM
Vestn Dermatol Venerol; 1981 May; (5):42-6. PubMed ID: 7293459
[No Abstract] [Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. [Dental agenesis in anhidrotic ectodermal dysplasia].
Fucci G; Ciccarelli R; Elefante R; Volpe A
Minerva Stomatol; 1984; 33(5):791-5. PubMed ID: 6596491
[No Abstract] [Full Text] [Related]
19. [Christ-Siemens-Touraine syndrome. Therapeutic case review].
Fraysse E; Fraysse H; Sebag F; Flach F; Damery C; Barnier G; Perrier D'Arc G
Rev Stomatol Chir Maxillofac; 1987; 88(3):185-9. PubMed ID: 3475762
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
