Exome sequencing as a differential diagnosis tool: Resolving mild trichohepatoenteric syndrome

D. Oz-Levi; B. Weiss; A. Lahad; S. Greenberger; B. Pode-Shakked; R. Somech; T. Olender; P. Tatarsky; D. Marek-Yagel; E. Pras; Y. Anikster; D. Lancet

doi:10.1111/cge.12494

Exome sequencing as a differential diagnosis tool: Resolving mild trichohepatoenteric syndrome

D. Oz-Levi
, B. Weiss
, A. Lahad
, S. Greenberger
, B. Pode-Shakked
, R. Somech
, T. Olender
, P. Tatarsky
, D. Marek-Yagel
, E. Pras
, Y. Anikster
, D. Lancet^*

^*Corresponding author for this work

Pediatrics

Weizmann Institute of Science
Sheba Medical Center at Tel Hashomer
The Edmond and Lily Safra Children's Hospital
The Gertner Institute

Research output: Contribution to journal › Letter › peer-review

14 Scopus citations

Original language	English
Pages (from-to)	602-603
Number of pages	2
Journal	Clinical Genetics
Volume	87
Issue number	6
DOIs	https://doi.org/10.1111/cge.12494
State	Published - 1 Jun 2015

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10.1111/cge.12494

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AU - Greenberger, S.

AU - Pode-Shakked, B.

AU - Somech, R.

AU - Olender, T.

AU - Tatarsky, P.

AU - Marek-Yagel, D.

AU - Pras, E.

AU - Anikster, Y.

AU - Lancet, D.

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Exome sequencing as a differential diagnosis tool: Resolving mild trichohepatoenteric syndrome

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