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• Anavi Y, Lerman P, Mintz S, Kiviti S (1989). Idiopathic familial gingival fibromatosis associated with mental retardation, epilepsy and hypertrichosis. Dev Med Child Neurol 31:538-542.
• Baumeister FA, Egger J, Schildhauer MT, Stengel-Rutkowski S (1993). Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22). Clin Genet 44(3):121-128.
• Baumeister FA, Schwarz HP, Stengel-Rutkowski S (1995). Childhood hypertrichosis: diagnosis and management. Arch Dis Child 72:457-459.
• Chadwick B, Hunter B, Hunter L, Aldred M, Wilkie A (1998). Laband syndrome: report of two cases, review of the literature, and identification of additional manifestations. Oral Surg Oral Med Oral Path Oral Radiol 78:57-63.
• Garcia-Cruz D, Sanchez-Corona J, Nazara Z, Garcia-Cruz MO, Figuera LE, Castaneda V, Cantu JM (1997). Congenital hypertrichosis, osteochondrodysplasia and cardiomegaly. Further delineation of a new genetic syndrome. Am J Med Genet 69:138-151.
• Gohlich-Ratmann G, Lackner A, Schaper J, Voit T, Gillessen-Kaesbach G (2000). Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition? Am J Med Genet 95:241-246.
• Guevara-Sangines E, Villalobos A, Vega-Memije ME, Mosqueda-Taylor A, Canun-Serrano S, Lacy-Niebla RM (2002). Congenital Generalized Terminal Hypertrichosis with Gingival Hyperplasia. Pediatr Dermatol 19:114-118.
• Irvine AD, Dolan OM, Hadden DR, Stewart FJ, Bingham EA, Nevin NC (1996). An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis. J Med Genet 33:972-974.
• Jalili IK (1989). Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition. J Med Genet 26:504-510.
• Judge MR, Khaw PT, Rice NS, Christopher A, Holmstrom G, Harper JI (1991). Congenital hypertrichosis lanuginosa and congenital glaucoma. Br J Dermatol 124:495-497.
• Kondoh T, Amamoto N, Hirota T, Kinoshita E, Moriuchi H, Matsumoto T, Shimono M, Kawakami A, Shirahata A (2003). Very long eyelashes, long eyebrows, sparse hair, and mental retardation in two unrelated boys: an atypical form of Oliver-McFarlane syndrome without retinal degeneration, or a new clinical entity? Am J Med Genet 120A:437-438.
• Martinez Santana S, Perez Alvarez F, Frias JL, Martinez-Frias ML (1993). Hypertrichosis, atrophic skin, ectropion, and macrostomia (Barber-Say syndrome): report of a new case. Am J Med Genet 47:20-23.
• Oliver GL, McFarlane DC (1965). Congenital trichomegaly with associated pigmentary degeneration of the retina, dwarfism and mental retardation. Arch Ophthal 74:169-171.
• Vashi RA, Mancini AJ, Paller AS (2001). Primary generalized and localized hypertrichosis in children. Arch Dermatol 137:877-884.