Congenital Cutis Laxa
Publisher
Springer New York
Reference43 articles.
1. Albrecht, B., de Brouwer, A. P., Lefeber, D. J., et al. (2010). MACS syndrome: A combined collagen and elastin disorder due to abnormal Golgi trafficking. American Journal of Medical Genetics. Part A, 152A, 2916–2918. 2. Andiran, N., Sarikayalar, F., Saraclar, M., et al. (2002). Autosomal recessive form of congenital cutis laxa: More than the clinical appearance. Pediatric Dermatology, 19, 412–414. 3. Banks, N. D., Redett, R. J., Mofid, M. Z., et al. (2003). Cutis laxa: Clinical experience and outcomes. Plastic and Reconstructive Surgery, 111, 2434–2442. 4. Basel-Vanagaite, L., Sarig, O., Hershkovitz, D., et al. (2009). RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome. American Journal of Human Genetics, 85, 254–263. 5. Beighton, P. (1972). The dominant and recessive forms of cutis laxa. Journal of Medical Genetics, 9, 216–221.
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