These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
89 related articles for article (PubMed ID: 4050864)
41. Cutaneous malignant melanoma and familial dysplastic nevi: evidence for autosomal dominance and pleiotropy. Bale SJ; Chakravarti A; Greene MH Am J Hum Genet; 1986 Feb; 38(2):188-96. PubMed ID: 3456198 [TBL] [Abstract][Full Text] [Related]
42. Treatment of congenital nevomelanocytic nevi with the CO2 and Q-switched alexandrite lasers. Chong SJ; Jeong E; Park HJ; Lee JY; Cho BK Dermatol Surg; 2005 May; 31(5):518-21. PubMed ID: 15962733 [TBL] [Abstract][Full Text] [Related]
43. Precursors to malignant melanoma. National Institutes of Health Consensus Development Conference Statement, Oct. 24-26, 1983. J Am Acad Dermatol; 1984 Apr; 10(4):683-8. PubMed ID: 6715623 [No Abstract] [Full Text] [Related]
44. [Birthmarks in Finnish newborns]. Pauli SL; Janas M; Marenk M; Kuokkanen K Duodecim; 1990; 106(7):571-7. PubMed ID: 1670213 [No Abstract] [Full Text] [Related]
45. Infantile myofibromatosis: two families supporting autosomal dominant inheritance. Smith A; Orchard D Australas J Dermatol; 2011 Aug; 52(3):214-7. PubMed ID: 21834820 [TBL] [Abstract][Full Text] [Related]
46. Familial nevus fusco-caeruleus zygomaticus. Yang B; Li L; Hu N; Li Y; Deng C Int J Dermatol; 2011 Jul; 50(7):858-9. PubMed ID: 21470213 [No Abstract] [Full Text] [Related]
47. Congenital pigmented and vascular lesions in newborn infants. Osburn K; Schosser RH; Everett MA J Am Acad Dermatol; 1987 Apr; 16(4):788-92. PubMed ID: 3571542 [TBL] [Abstract][Full Text] [Related]
48. Infantile myofibromatosis: report on a family with autosomal dominant inheritance and variable penetrance. Kulkarni K; Desai S; Grundy P; Sergi C J Pediatr Surg; 2012 Dec; 47(12):2312-5. PubMed ID: 23217896 [TBL] [Abstract][Full Text] [Related]
51. Congenital nevi: accuracy of relative area index measurements. Enhamre A Arch Dermatol; 1987 Jun; 123(6):709-10. PubMed ID: 3579349 [No Abstract] [Full Text] [Related]
52. Familial multiple pigmented naevi and sensorineural deafness. A new autosomal dominant syndrome? Peserico A; Martini A; Tenconi R Int J Pediatr Otorhinolaryngol; 1981 Sep; 3(3):269-72. PubMed ID: 7319705 [No Abstract] [Full Text] [Related]
53. Early-onset nevi. Williams ML Pediatr Dermatol; 1993 Jun; 10(2):198. PubMed ID: 8346122 [No Abstract] [Full Text] [Related]
54. Incidence of depigmented nevi in 1,000 healthy term newborns. Kennedy JL; Kalish GH Mod Probl Paediatr; 1975; 17():211. PubMed ID: 1186677 [No Abstract] [Full Text] [Related]
55. Autosomal dominant inheritance of infantile myofibromatosis. Zand DJ; Huff D; Everman D; Russell K; Saitta S; McDonald-McGinn D; Zackai EH Am J Med Genet A; 2004 Apr; 126A(3):261-6. PubMed ID: 15054839 [TBL] [Abstract][Full Text] [Related]
56. Prevalence of naevocytic naevi after chemotherapy for childhood cancer. de Wit PE; de Vaan GA; de Boo TM; Lemmens WA; Rampen FH Med Pediatr Oncol; 1990; 18(4):336-8. PubMed ID: 2355895 [TBL] [Abstract][Full Text] [Related]
57. Familial nevus flammeus of the forehead and Unna's nevus. Merlob P; Reisner SH Clin Genet; 1985 Feb; 27(2):165-6. PubMed ID: 3978851 [TBL] [Abstract][Full Text] [Related]