185 related articles for article (PubMed ID: 469901)
1. X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency.
Filippi G; Rinaldi A; Crisponi G; Daniels GL; Siniscalco M
J Med Genet; 1979 Jun; 16(3):223-4. PubMed ID: 469901
[TBL] [Abstract][Full Text] [Related]
2. Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker.
Hanauer A; Alembik Y; Arveiler B; Formiga L; Gilgenkrantz S; Mandel JL
Hum Genet; 1988 Oct; 80(2):177-80. PubMed ID: 2902000
[TBL] [Abstract][Full Text] [Related]
3. Absence of close linkage between the locus for Xg and the locus for anhidrotic ectodermal dysplasia.
Simpson JL; Allen FH; New M; German J
Vox Sang; 1969 Nov; 17(5):465-7. PubMed ID: 5360160
[No Abstract] [Full Text] [Related]
4. Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.
Filippi G; Rinaldi A; Palmarino R; Seravalli E; Siniscalco M
Genetics; 1977 May; 86(1):199-212. PubMed ID: 301840
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm.
Purrello M; Nussbaum R; Rinaldi A; Filippi G; Traccis S; Latte B; Siniscalco M
Hum Genet; 1984; 65(3):295-9. PubMed ID: 6321326
[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. Anhidrotic (or hypohidrotic) ectodermal dysplasis.
Martin-Pascual A; De Unamuno P; Aparicio M; Herreros V
Dermatologica; 1977; 154(4):235-43. PubMed ID: 140825
[No Abstract] [Full Text] [Related]
9. [The type of inheritance of anhidrotic ectodermal dysplasia].
Al'tshuler BA; Suvorova KN
Vestn Dermatol Venerol; 1984 Feb; (2):15-8. PubMed ID: 6720063
[No Abstract] [Full Text] [Related]
10. 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]
11. [A typical cases of X-linked anhidrotic ectodermal dysplasia and a diagnosis of carriers].
Yamamoto Y; Fugisawa S; Morishima T; Morioka S; Iinuma K
Nihon Hifuka Gakkai Zasshi; 1990 Mar; 100(4):527-32. PubMed ID: 2370706
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.
Rinaldi A; Filippi G; Siniscalco M
Am J Hum Genet; 1976 Sep; 28(5):496-505. PubMed ID: 984045
[TBL] [Abstract][Full Text] [Related]
14. X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization.
Clarke A; Sarfarazi M; Thomas NS; Roberts K; Harper PS
Hum Genet; 1987 Apr; 75(4):378-80. PubMed ID: 2883107
[TBL] [Abstract][Full Text] [Related]
15. Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis.
Zonana J; Sarfarazi M; Thomas NS; Clarke A; Marymee K; Harper PS
J Pediatr; 1989 Mar; 114(3):392-9. PubMed ID: 2564048
[TBL] [Abstract][Full Text] [Related]
16. Hypohidrotic ectodermal dysplasia.
Clarke A
J Med Genet; 1987 Nov; 24(11):659-63. PubMed ID: 3323518
[No Abstract] [Full Text] [Related]
17. Further evidence against linkage between Christ-Siemens-Touraine (CST) and XG loci.
Chautard-Freire-Maia EA; Primo-Parmo SL; Pinheiro M; Freire-Maia N
Hum Genet; 1981; 57(2):205-6. PubMed ID: 7194846
[No Abstract] [Full Text] [Related]
18. Identifying carriers for X-linked hypohidrotic ectodermal dysplasia.
Pinheiro M; Freire-Maia N
Lancet; 1977 Oct; 2(8044):936. PubMed ID: 72281
[No Abstract] [Full Text] [Related]
19. Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12.
Kølvraa S; Kruse TA; Jensen PK; Linde KH; Vestergaard SR; Bolund L
Hum Genet; 1986 Nov; 74(3):284-7. PubMed ID: 2877938
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis.
Zonana J; Schinzel A; Upadhyaya M; Thomas NS; Anton-Lamprecht I; Harper PS
Am J Med Genet; 1990 Jan; 35(1):132-5. PubMed ID: 2301463
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
