A male infant with Xq22.2q22.3 duplication containingPLP1andMID2-Reference-Cited by-同舟云学术

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A male infant with Xq22.2q22.3 duplication containingPLP1andMID2

Published:2020-01-17 Issue:3 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Chanchani Swati R.¹,Xie Hongyan²,Sekhon Gurbax³,Melikishvili Ana M.⁴,Moyer Harasink Sue¹,Pall Harpreet¹,Giampietro Philip F.⁵^ORCID

Affiliation:

1. Department of Pediatrics St. Christopher's Hospital for Children Drexel University College of Medicine Philadelphia PA USA

2. Tricore Reference Laboratory Albuquerque NM USA

3. Integrated Genetics NM Santa Fe USA

4. A. I. Dupont Hospital Wilmington DE USA

5. Rutgers‐Robert Wood Johnson Medical School New Brunswick NJ USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1078

Reference46 articles.

2. AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis

3. Modulation of T-cell activation by the glucocorticoid-induced leucine zipper factor via inhibition of nuclear factor κB

4. Thymosin β15: A novel regulator of tumor cell motility upregulated in metastatic prostate cancer

5. Identification of a Gene That Reverses the Immortal Phenotype of a Subset of Cells and Is a Member of a Novel Family of Transcription Factor-Like Genes

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1. Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome;Genes;2023-03-09

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