Craniosynostosis in the Amish

Author:

Cross Harold E.,Opitz John M.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Premature closure of the cranial sutures;Simmons;J. Pediat.,1947

2. Über den Cretinismus, namentlich in Franken und über pathologische Schädelformen;Virchow;Verhandl. Phys.-Med. Ges. Wurzburg,1851

3. Clinical studies in craniosynostosis. Analyses of fifty cases and descriptions of a method of surgical treatment;Ingraham;Surgery,1948

4. Importance of early surgical treatment of craniosynostosis. Review of 36 cases treated during first six months of life;McLaurin;Pediatrics,1952

5. Human genetics;Gates,1946

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1. Fibroblast Growth Factor Receptor and Related Skeletal Disorders;Molecular Pathology in Clinical Practice;2016

2. Mutations in the interleukin receptor IL 11 RA cause autosomal recessive Crouzon‐like craniosynostosis;Molecular Genetics & Genomic Medicine;2013-08-19

3. Familial Inheritance of Coronal Craniosynostosis;Developmental Medicine & Child Neurology;2008-11-12

4. Germinal mosaicism in Crouzon syndrome;Clinical Genetics;2008-06-28

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