PITX2 and FOXC1 spectrum of mutations in ocular syndromes

L.M. Reis; R.C. Tyler; B.A.V. Kloss; K.F. Schilter; A.V. Levin; R.B. Lowry; P.J.G. Zwijnenburg; E. Stroh; U. Broeckel; J.C. Murray; E.V. Semina

doi:10.1038/ejhg.2012.80

PITX2 and FOXC1 spectrum of mutations in ocular syndromes

L.M. Reis
, R.C. Tyler
, B.A.V. Kloss
, K.F. Schilter
, A.V. Levin
, R.B. Lowry
, P.J.G. Zwijnenburg
, E. Stroh
, U. Broeckel
, J.C. Murray
, E.V. Semina

Research output: Contribution to journal › Article › Academic › peer-review

Original language	Undefined/Unknown
Pages (from-to)	1224-1233
Journal	European journal of human genetics
Volume	20
Issue number	12
DOIs	https://doi.org/10.1038/ejhg.2012.80
Publication status	Published - 2012

Access to Document

10.1038/ejhg.2012.80

Cite this

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title = "PITX2 and FOXC1 spectrum of mutations in ocular syndromes",

author = "L.M. Reis and R.C. Tyler and B.A.V. Kloss and K.F. Schilter and A.V. Levin and R.B. Lowry and P.J.G. Zwijnenburg and E. Stroh and U. Broeckel and J.C. Murray and E.V. Semina",

year = "2012",

doi = "10.1038/ejhg.2012.80",

language = "Undefined/Unknown",

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pages = "1224--1233",

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AU - Reis, L.M.

AU - Tyler, R.C.

AU - Kloss, B.A.V.

AU - Schilter, K.F.

AU - Levin, A.V.

AU - Lowry, R.B.

AU - Zwijnenburg, P.J.G.

AU - Stroh, E.

AU - Broeckel, U.

AU - Murray, J.C.

AU - Semina, E.V.

PY - 2012

Y1 - 2012

U2 - 10.1038/ejhg.2012.80

DO - 10.1038/ejhg.2012.80

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SN - 1018-4813

VL - 20

SP - 1224

EP - 1233

JO - European journal of human genetics

JF - European journal of human genetics

IS - 12

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