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| | 1 - 10 of 192 journal articles in the PubMed database | Email to a friend | | |
| Koppe R, Kaplan P, Hunter A, et al.
Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome). [Case Reports, Journal Article]
Am J Med Genet 1989 Nov; 34(3):305-12.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Vaccaro M, Salpietro DC, Briuglia S, et al.
Cutis laxa in Kabuki make-up syndrome. [Case Reports, Journal Article]
J Am Acad Dermatol 2005 Nov; 53(5 Suppl 1):S247-51.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kunze J, Majewski F, Montgomery P, et al.
De Barsy syndrome--an autosomal recessive, progeroid syndrome. [Journal Article]
Eur J Pediatr 1985 Nov; 144(4):348-54.
Abstract | Full Citation | Find Related Articles | | Borochowitz Z, Pavone L, Mazor G, et al.
New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement. [Case Reports, Journal Article, Review]
Am J Med Genet 1992 Jul 1; 43(4):678-85.
Abstract | Full Citation | Find Related Articles | | Rybojad M, Baumann C, Godeau G, et al.
[Congenital generalized cutis laxa: 5 cases] [Case Reports, Journal Article]
Ann Dermatol Venereol 1999 Apr; 126(4):317-9.
Abstract | Full Citation | Find Related Articles | | Khalifa MM, Cappon S, Soboleski D, et al.
New mental retardation syndrome associated with ocular colobomas, cleft palate, and genital, skeletal, and craniofacial abnormalities. [Case Reports, Journal Article]
Am J Med Genet 2002 Jan 22; 107(3):237-42.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Biver A, De Rijcke S, Toppet V, et al.
Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defects. [Case Reports, Journal Article, Review]
Clin Genet 1994 Jun; 45(6):318-22.
Abstract | Full Citation | Find Related Articles | | Imaizumi K, Kurosawa K, Makita Y, et al.
Male with type II autosomal recessive cutis laxa. [Case Reports, Journal Article]
Clin Genet 1994 Jan; 45(1):40-3.
Abstract | Full Citation | Find Related Articles | | Hucthagowder V, Sausgruber N, Kim KH, et al.
Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. [Journal Article]
Am J Hum Genet 2006 Jun; 78(6):1075-80.
Abstract | Full Citation | Publisher Full Text | Find Related Articles |   |
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