Dysmorphic Syndromes with Anomalies of the Skull and Extremities
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Publisher
Springer Nature Switzerland
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-39347-1_26
Reference10 articles.
1. Cohen DM, Green JG, Miller J, Gorlin RJ, Reed JA. Acrocephalopolysyndactyly type II - Carpenter syndrome: Clinical spectrum and an attempt at unification with Goodman and summit syndromes. Am J Med Genet. 1987;28(2):311–24.
2. Robinow M, Sorauf TJ. Acrocephalopolysyndactyly, type Noack, in a large kindred. Birth Defects Orig Artic Ser. 1975;11(5):99–106.
3. Sakati N, Nyhan WL, Tisdale WK. A new syndrome with acrocephalopolysyndactyly, cardiac disease, and distinctive defects of the ear, skin, and lower limbs. J Pediatr. 1971;79(1):104–9.
4. Werner H, Castro P, Daltra P, Lopes J, Ribeiro G, Araujo JE. Prenatal diagnosis of Apert syndrome using ultrasound, magnetic resonanceimaging, and three-dimensional virtual / physical models: three case series and literature review. Childs Nerv Syst. 2018;34(8):1563–71.
5. Fernandes MB, Maximino LP, Perosa GB, Abramides DV, Passos-Bueno MR, Yacubian-Fernandes A. Apert and Crouzon syndromes-Cognitive development, brain abnormalities, and molecular aspects. Am J Med Genet A. 2016;170(6):1532–7.
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