De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability

Author:

Brett Maggie S.,Ng Ivy S.L.,Lim Eileen C.P.,Yong Min Hwee,Li Zhihui,Lai Angeline,Tan Ene-Choo

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference35 articles.

1. Anesthesia for a child with deletion 3q syndrome;Almenrader;Paediatr. Anaesth.,2008

2. A case report of partial deletion of the long arm of the no. 3 chromosome;Arai;Med. Genet. Res.,1982

3. FOXL2 mutations and genomic rearrangements in BPES;Beysen;Hum. Mutat.,2009

4. Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic features;Brueton;J. Med. Genet.,1989

5. Detection of an interstitial 3q21.1–q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia;Callier;Am. J. Med. Genet. A,2009

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