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F Silan
F Silan
Genetics
Phenotype
Frameshift mutation
SALL4
Molecular genetics
2
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72
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Two Siblings with Currarino Syndrome with 7q34 Deletion Due to Maternal t(7;14)(q34;p13)
2014
F Silan
D Kuru
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SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism
2004
Journal of Medical Genetics
Wiktor Borozdin
Detlef Boehm
Michael Leipoldt
Christian Wilhelm
William Reardon
Jill Clayton-Smith
K. Becker
H. Mühlendyck
Robin M. Winter
Ö Giray
F Silan
Jürgen Kohlhase
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Citations (72)
1