Standard
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome). / Kjær, Klaus Wilbrandt; Hansen, Lars; Schwabe, G.C.; Marques-de-Faria, A.P.; Eiberg, Hans Rudolf Lytchoff; Mundlos, S.; Tommerup, Niels; Rosenberg, T.
In:
Journal of Medical Genetics, No. Vol. 42, 2005, p. 292-298.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Kjær, KW, Hansen, L, Schwabe, GC, Marques-de-Faria, AP, Eiberg, HRL, Mundlos, S, Tommerup, N & Rosenberg, T 2005, 'Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)', Journal of Medical Genetics, no. Vol. 42, pp. 292-298.
APA
Kjær, K. W., Hansen, L., Schwabe, G. C., Marques-de-Faria, A. P., Eiberg, H. R. L., Mundlos, S., Tommerup, N., & Rosenberg, T. (2005). Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome). Journal of Medical Genetics, (Vol. 42), 292-298.
Vancouver
Kjær KW, Hansen L, Schwabe GC, Marques-de-Faria AP, Eiberg HRL, Mundlos S et al. Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome). Journal of Medical Genetics. 2005;(Vol. 42):292-298.
Author
Kjær, Klaus Wilbrandt ; Hansen, Lars ; Schwabe, G.C. ; Marques-de-Faria, A.P. ; Eiberg, Hans Rudolf Lytchoff ; Mundlos, S. ; Tommerup, Niels ; Rosenberg, T. / Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome). In: Journal of Medical Genetics. 2005 ; No. Vol. 42. pp. 292-298.
Bibtex
@article{764e017074c311dbbee902004c4f4f50,
title = "Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)",
author = "Kj{\ae}r, {Klaus Wilbrandt} and Lars Hansen and G.C. Schwabe and A.P. Marques-de-Faria and Eiberg, {Hans Rudolf Lytchoff} and S. Mundlos and Niels Tommerup and T. Rosenberg",
year = "2005",
language = "English",
pages = "292--298",
journal = "Journal of Medical Genetics",
issn = "0022-2593",
publisher = "B M J Group",
number = "Vol. 42",
}
RIS
TY - JOUR
T1 - Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)
AU - Kjær, Klaus Wilbrandt
AU - Hansen, Lars
AU - Schwabe, G.C.
AU - Marques-de-Faria, A.P.
AU - Eiberg, Hans Rudolf Lytchoff
AU - Mundlos, S.
AU - Tommerup, Niels
AU - Rosenberg, T.
PY - 2005
Y1 - 2005
M3 - Journal article
SP - 292
EP - 298
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
SN - 0022-2593
IS - Vol. 42
ER -
