158 related articles for article (PubMed ID: 9034652)
1. Genodermatoses in women.
Mevorah B; Politi Y
Clin Dermatol; 1997; 15(1):17-29. PubMed ID: 9034652
[No Abstract] [Full Text] [Related]
2. The lines of Blaschko: a developmental pattern visualizing functional X-chromosome mosaicism.
Happle R
Curr Probl Dermatol; 1987; 17():5-18. PubMed ID: 3595192
[No Abstract] [Full Text] [Related]
3. X-linked dominant chondrodysplasia punctata: a peroxisomal disorder?
Wilson CJ; Aftimos S
Am J Med Genet; 1998 Jul; 78(3):300-2. PubMed ID: 9677071
[TBL] [Abstract][Full Text] [Related]
4. Generalized epidermolytic hyperkeratosis in a child born to a parent with systematized epidermolytic linear epidermal nevus.
Reddy BS; Thadeus J; Kumar SK; Jaishanker T; Garg BR
Int J Dermatol; 1997 Mar; 36(3):198-200. PubMed ID: 9159002
[No Abstract] [Full Text] [Related]
5. [Genetic interpretation of linear skin abnormalities].
Happle R
Hautarzt; 1978 Jul; 29(7):357-63. PubMed ID: 567211
[TBL] [Abstract][Full Text] [Related]
6. Clinical variation in X-linked dominant chondrodysplasia punctata (X-linked dominant ichthyosis).
Feldmeyer L; Mevorah B; Grzeschik KH; Huber M; Hohl D
Br J Dermatol; 2006 Apr; 154(4):766-9. PubMed ID: 16536827
[No Abstract] [Full Text] [Related]
7. Incontinentia pigmenti (Bloch-Sulzberger syndrome).
Landy SJ; Donnai D
J Med Genet; 1993 Jan; 30(1):53-9. PubMed ID: 8423608
[No Abstract] [Full Text] [Related]
8. X-linked dominant inherited diseases with lethality in hemizygous males.
Wettke-Schäfer R; Kantner G
Hum Genet; 1983; 64(1):1-23. PubMed ID: 6873941
[TBL] [Abstract][Full Text] [Related]
9. Neurocutaneous disorders.
Barbagallo JS; Kolodzieh MS; Silverberg NB; Weinberg JM
Dermatol Clin; 2002 Jul; 20(3):547-60, viii. PubMed ID: 12170887
[TBL] [Abstract][Full Text] [Related]
10. Linear and whorled pigmentation.
Harre J; Millikan LE
Int J Dermatol; 1994 Aug; 33(8):529-37. PubMed ID: 7960343
[No Abstract] [Full Text] [Related]
11. An unusual rash in a neonate. X-linked dominant ichthyosis (XLDI).
Moriarty B; Bourke JF; Fitzgibbon J; Irvine AD
Clin Exp Dermatol; 2010 Apr; 35(3):e62-4. PubMed ID: 20500184
[No Abstract] [Full Text] [Related]
12. Lyonization and the lines of Blaschko.
Happle R
Hum Genet; 1985; 70(3):200-6. PubMed ID: 3894210
[TBL] [Abstract][Full Text] [Related]
13. Histologic and ultrastructural features of the ichthyotic skin in X-linked dominant chondrodysplasia punctata.
Kolde G; Happle R
Acta Derm Venereol; 1984; 64(5):389-94. PubMed ID: 6208716
[TBL] [Abstract][Full Text] [Related]
14. Palmar papillomatous lesions reminiscent of epidermal nevus in a case of focal dermal hypoplasia: a nosological consideration.
van der Steen PH; Mittag H; Küster W; Happle R
Dermatology; 1996; 193(2):147-8. PubMed ID: 8884155
[TBL] [Abstract][Full Text] [Related]
15. Lethal course of X-linked dominant chondrodysplasia punctata in a male newborn.
De Raeve L; Song M; De Dobbeleer G; Spehl M; Van Regemorter N
Dermatologica; 1989; 178(3):167-70. PubMed ID: 2566519
[TBL] [Abstract][Full Text] [Related]
16. A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval.
Klink A; Meindl A; Hellebrand H; Rappold GA
Hum Genet; 1994 Apr; 93(4):463-6. PubMed ID: 8168818
[TBL] [Abstract][Full Text] [Related]
17. Dominant sex-linked inherited chondrodysplasia punctata: a distinct type of chondrodysplasia punctata.
Manzke H; Christophers E; Wiedemann HR
Clin Genet; 1980 Feb; 17(2):97-107. PubMed ID: 7363504
[TBL] [Abstract][Full Text] [Related]
18. Incidental epidermolytic hyperkeratosis.
Mahaisavariya P; Cohen PR; Rapini RP
Am J Dermatopathol; 1995 Feb; 17(1):23-8. PubMed ID: 7695008
[TBL] [Abstract][Full Text] [Related]
19. [X-chromosome dominant chondrodysplasia punctata (Happle syndrome). Lyonization of the eyelashes?].
Wollina U; Vogel H
Hautarzt; 1994 Jan; 45(1):42-4. PubMed ID: 8150617
[TBL] [Abstract][Full Text] [Related]
20. X-linked dominant chondrodysplasia punctata/ichthyosis/cataract syndrome in males.
Happle R
Am J Med Genet; 1995 Jul; 57(3):493. PubMed ID: 7677158
[No Abstract] [Full Text] [Related]
[Next] [New Search]
