Response to Phelan K. et al.: letter to the editor regarding Disciglio et al: interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome

Am J Med Genet A. 2015 Jul;167(7):1681. doi: 10.1002/ajmg.a.36894. Epub 2015 May 5.

Authors

Francesca Mari^{1

2}, Antonio Novelli³, Corrado Romano⁴, Alessandra Renieri^{1

2}

Affiliations

¹ Medical Genetics, University of Siena, Siena, Italy.
² Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
³ IRCCS Casa Sollievo della Sofferenza Hospital, Mendel Institute, Rome, Italy.
⁴ Unit of Pediatrics and Medical Genetics, IRCCS Associazione Oasi Maria Santissima, Troina, Italy.

PMID: 25944375
DOI: 10.1002/ajmg.a.36894

No abstract available

Publication types

Letter
Comment

MeSH terms

Chromosome Deletion*
Chromosome Disorders / diagnosis*
Chromosome Disorders / genetics*
Chromosomes, Human, Pair 22*
Female
Humans
Male
Nerve Tissue Proteins / genetics*

Substances

Nerve Tissue Proteins