161 related articles for article (PubMed ID: 6946797)
1. 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]
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. 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]
4. Manifestation of the lines of Blaschko in women heterozygous for X-linked hypohidrotic ectodermal dysplasia.
Happle R; Frosch PJ
Clin Genet; 1985 May; 27(5):468-71. PubMed ID: 4006271
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. 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]
7. 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]
8. 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]
9. Hypohidrotic ectodermal dysplasia.
Clarke A
J Med Genet; 1987 Nov; 24(11):659-63. PubMed ID: 3323518
[No Abstract] [Full Text] [Related]
10. 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]
11. 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]
12. [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]
13. Sweat pore counts in ectodermal dysplasias.
Kleinebrecht J; Degenhardt KH; Grubisic A; Günther E; Svejcar J
Hum Genet; 1981; 57(4):437-9. PubMed ID: 7286987
[No Abstract] [Full Text] [Related]
14. Identification of functioning sweat pores and visualization of skin temperature patterns in X-linked hypohidrotic ectodermal dysplasia by whole body thermography.
Clark RP; Goff MR; MacDermot KD
Hum Genet; 1990 Nov; 86(1):7-13. PubMed ID: 2253940
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Hypodontia, ectodermal dysplasia and sweat pore count.
Tso MS; Crawford PJ; Miller J
Br Dent J; 1985 Jan; 158(2):56-60. PubMed ID: 3855640
[No Abstract] [Full Text] [Related]
17. Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications.
Ferguson BM; Thomas NS; Munoz F; Morgan D; Clarke A; Zonana J
J Med Genet; 1998 Feb; 35(2):112-5. PubMed ID: 9507389
[TBL] [Abstract][Full Text] [Related]
18. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia.
Clarke A; Phillips DI; Brown R; Harper PS
Arch Dis Child; 1987 Oct; 62(10):989-96. PubMed ID: 2445301
[TBL] [Abstract][Full Text] [Related]
19. A simple technique for recording and counting sweat pores on the dermal ridges.
O'Leary E; Slaney J; Bryant DG; Fraser FC
Clin Genet; 1986 Feb; 29(2):122-8. PubMed ID: 3955862
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
