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5. Adams-Oliver syndrome: new evidence in variable expressivity? Girish M; Mujawar N; Anekar U; Bhattad S Int J Dermatol; 2014 Jul; 53(7):891-3. PubMed ID: 24372423 [No Abstract] [Full Text] [Related]
6. Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions. Zlotogorski A; Panteleyev AA; Aita VM; Christiano AM J Invest Dermatol; 2002 May; 118(5):887-90. PubMed ID: 11982770 [TBL] [Abstract][Full Text] [Related]
7. [Little-Lassueur syndrome in a father and daughter]. Egorov NA; Trezubov VN; Volkov VP Vestn Dermatol Venerol; 1985 Oct; (10):63-6. PubMed ID: 4082773 [No Abstract] [Full Text] [Related]
8. Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions. Zlotogorski A; Panteleyev AA; Aita VM; Christiano AM J Invest Dermatol; 2001 Dec; 117(6):1662-5. PubMed ID: 11886538 [TBL] [Abstract][Full Text] [Related]
9. [Mastocytosis in a brother and sister, with pseudopeladic localization in the scalp, in the sister]. Bureau Y; Barrière H; Litoux P; Bureau B Bull Soc Fr Dermatol Syphiligr; 1971; 78(3):240-1. PubMed ID: 5134963 [No Abstract] [Full Text] [Related]
10. Congenital absence of a patch of skin on the scalp. Simon MW Am Fam Physician; 1994 Dec; 50(8):1653-4. PubMed ID: 7976995 [No Abstract] [Full Text] [Related]
11. Congenital atrichia with nail dystrophy, abnormal facies, and retarded psychomotor development in two siblings: a new autosomal recessive syndrome? Vogt BR; Traupe H; Hamm H Pediatr Dermatol; 1988 Nov; 5(4):236-42. PubMed ID: 2466283 [TBL] [Abstract][Full Text] [Related]
12. Pseudopelade of Brocq in two brothers: possible role of hereditary factors in the pathogenesis. Singh S; De D; Saikia UN; Kanwar AJ Indian J Dermatol Venereol Leprol; 2012; 78(5):637-40. PubMed ID: 22960824 [No Abstract] [Full Text] [Related]
13. Autosomal recessive inheritance of atrichia congenita. Cantú JM; Sánchez-Corona J; González-Mendoza A; Martínez y Martínez R; García-Cruz D Clin Genet; 1980; 17(3):209-12. PubMed ID: 7363508 [TBL] [Abstract][Full Text] [Related]
14. Congenital Hypotrichosis and Congenital Atrichia. Al-Dawsari NA; Kaliyadan F Skinmed; 2018; 16(1):27-32. PubMed ID: 29551108 [TBL] [Abstract][Full Text] [Related]
16. Of hairless mice and men: the genetic basis of congenital alopecia universalis/congenital atrichia. Bale SJ J Cutan Med Surg; 1999 Oct; 3(6):309-11. PubMed ID: 10575161 [TBL] [Abstract][Full Text] [Related]
17. Atrichia with papular lesions: electron microscopic observations of cystic lesions. Nomura K; Hashimoto I; Takahashi G; Ito M Am J Dermatopathol; 2001 Jun; 23(3):227-31. PubMed ID: 11391105 [TBL] [Abstract][Full Text] [Related]
18. Atrichias and hypotrichoses: a brief review with description of a recessive atrichia in two brothers. Pinheiro M; Freire-Maia N Hum Hered; 1985; 35(1):53-5. PubMed ID: 3972425 [No Abstract] [Full Text] [Related]
19. [Congenital ichthyosiform erythroderma with cicatrical alopecia of the scalp]. Longhin S; Muresan D; Wolfshaut A Arch Belg Dermatol Syphiligr; 1968; 24(1):1-11. PubMed ID: 5759524 [No Abstract] [Full Text] [Related]
20. A recurrent splice-site mutation in the human hairless gene underlies congenital atrichia in Irish families. O'Regan GM; Zurada J; Martinez-Mir A; Christiano AM; Irvine AD Br J Dermatol; 2007 Apr; 156(4):744-7. PubMed ID: 17263802 [No Abstract] [Full Text] [Related] [Next] [New Search]