Germinal mosaicism in Crouzon syndrome. A family with three affected siblings of normal parents

Author:

Navarrete Carmen,Peña Ramón,Peñaloza Rosenda,Salamanca Fabio

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. Germinal mosaicism in Apert syndrome;Allanson;Clin. Genet.,1986

2. Hereditary craniofacial dysostosis, or Crouzon's disease;Atkinson;Med. Press Circular,1937

3. Acrocephalosyndactyly type III: Chotzen's syndrome;Bartsocas;J. Pediatr.,1970

4. Achondroplasia in two sisters with normal parents;Bowen;Birth Defects,1974

5. A family study of craniosynostosis, with probable recognition of a distinct syndrome;Carter;J. Med. Genet.,1982

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1. Crouzon Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

2. Family of Crouzon Syndrome Represents the Evolution of the Frontofacial Monobloc Advancement Technique;Journal of Craniofacial Surgery;2015-09

3. Crouzon Syndrome;Atlas of Genetic Diagnosis and Counseling;2015

4. Craniosynostosis;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

5. Crouzon Syndrome;Atlas of Genetic Diagnosis and Counseling;2012

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