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Article Details
- Journal Title
- Case Reports in Genetics
- Volume
- 2014
- Article Title
- A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability
- List of Authors
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- Farmaditya E. P. Mundhofir
- Rolph Pfundt(ORCID ID: http://orcid.org/0000-0002-0584-4398)
- Nico Leijsten(ORCID ID: http://orcid.org/0000-0002-1003-2861)
- Willy Nillesen
- Sultana M. H. Faradz
- Nicole de Leeuw(ORCID ID: http://orcid.org/0000-0002-9796-3342)
- Article ID
- 530134
- Article Type
- Case Report
- No. of Pages
- 5 Pages
- Additional Authors
Invoice Details
- Invoice Issue Date
- 26 April 2024
- Type of Reprints
- Colored, Covered
- Invoice Ref. No.
- Terms
- Payable upon Receipt
Charges
- No. of Copies
- Reprints Charges
- 0.00
- Total
- $