Merve Celenkoglu Tombak on Muck Rack

Merve Celenkoglu Tombak

As seen in: Wiley Online Library
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Articles

Filippi syndrome: Three new families suggest that urinary system abnormalities may belong to clinical spectrum of the disease

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By Intergen Genetics, Ceren Damla Durmaz, Merve Celenkoglu Tombak, Gökhan Çetin
| pericles.pericles-prod.literatumonline.com
CONFLICT OF INTEREST STATEMENT The authors declare no conflicts of interest. REFERENCES , , , & (2008). Filippi syndrome: Further clinical characterization. American Journal of Medical Genetics Part A, 146A, 1848–1852. , , , , , , , , & (2018). CKAP2L mutation confirms the diagnosis of Filippi syndrome. Clinical Genetics, 93, 1109–1110. , , & (1985). Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome? American Journal of Medical Genetics, 22, 821–824.
Open in Who Shared Issue with article?

Filippi syndrome: Three new families suggest that urinary system abnormalities may belong to clinical spectrum of the disease

|
By Intergen Genetics, Ceren Damla Durmaz, Merve Celenkoglu Tombak, Gökhan Çetin
| Wiley Online Library
CONFLICT OF INTEREST STATEMENT The authors declare no conflicts of interest. REFERENCES , , , & (2008). Filippi syndrome: Further clinical characterization. American Journal of Medical Genetics Part A, 146A, 1848–1852. , , , , , , , , & (2018). CKAP2L mutation confirms the diagnosis of Filippi syndrome. Clinical Genetics, 93, 1109–1110. , , & (1985). Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome? American Journal of Medical Genetics, 22, 821–824.
Open in Who Shared Issue with article?
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