Dysmorphic Syndromes with Anomalies of the Oral Cavity and Extremities
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Publisher
Springer Nature Switzerland
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-39347-1_27
Reference11 articles.
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2. Kantaputra PN, Dejkhamron P, Intachai W, Ngamphiw C, Kawasaki K, Ohazama A, Krisanaprakornkit S, Olsen B, Tongsima S, Ketudat Cairns JR. Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2. Eur J Orthod. 2020;43(1):45–50.
3. Miller DE, Chow P, Gallagher ER, Perkins JA, Wenger TL. Catel-Manzke syndrome without Manzke dysostosis. Am J Med Genet A. 2020;182(3):437–40.
4. Clarkson JH, Homfray T, Heron CW, Moss AL. Catel-Manzke syndrome: a case report of a female with severely malformed hands and feet An extension of the phenotype or a new syndrome? Clin Dysmorphol. 2004;13(4):237–40.
5. Rosselli D, Gulienetti R. Ectodermal dysplasia. Br J Plast Surg. 1961;14:190–204.
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