Dual genetic diagnoses: Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations inHOXA13andNRXN1-Reference-Cited by-同舟云学术

Dual genetic diagnoses: Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations inHOXA13andNRXN1

Author:

Wallis Mathew¹,Tsurusaki Yoshinori²,Burgess Trent³⁴,Borzi Peter⁵,Matsumoto Naomichi²,Miyake Noriko²,True Deanna⁶,Patel Chirag¹

Affiliation:

1. Genetic Health Queensland; Royal Brisbane and Women's Hospital; Brisbane Queensland Australia

2. Department of Human Genetics; Yokohama City University Graduate School of Medicine; Yokohama Japan

3. Victorian Clinical Genetics Service; MCRI, Royal Children's Hospital; Parkville Victoria Australia

4. Department of Paediatrics; Royal Children's Hospital; University of Melbourne; Parkville Victoria Australia

5. Department of Paediatric Surgery and Urology; Lady Cilento Children's Hospital; South Brisbane Queensland Australia

6. Department of General Paediatrics; Lady Cilento Children's Hospital; South Brisbane Queensland Australia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference28 articles.

3. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders;Ching;Am J Med Genet Part B Neuropsychiatr Genet,2010

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