p63 mutations account for a range of congenital anomaly syndromes with a clear genotype phenotype correlation

H Brunner; J A McGrath; J Celli; P Duijf; F Gurrieri; F McKeon; P Propping; M Bamshad; H van Bokhoven; B Hamel; G Neri; V Doetsch; R de Waal; A Yang; K Vanmolkot

p63 mutations account for a range of congenital anomaly syndromes with a clear genotype phenotype correlation

H Brunner, J A McGrath, J Celli, P Duijf, F Gurrieri, F McKeon, P Propping, M Bamshad, H van Bokhoven, B Hamel, G Neri, V Doetsch, R de Waal, A Yang, K Vanmolkot

Dermatology

Research output: Contribution to journal › Meeting abstract

Original language	English
Pages (from-to)	S27 - S27
Journal	Journal of Medical Genetics
Volume	37
Publication status	Published - 2000

Cite this

@article{d8cc2dd053194dfa935234c7910c391d,

title = "p63 mutations account for a range of congenital anomaly syndromes with a clear genotype phenotype correlation",

author = "H Brunner and McGrath, {J A} and J Celli and P Duijf and F Gurrieri and F McKeon and P Propping and M Bamshad and {van Bokhoven}, H and B Hamel and G Neri and V Doetsch and {de Waal}, R and A Yang and K Vanmolkot",

year = "2000",

language = "English",

volume = "37",

pages = "S27 -- S27",

journal = "Journal of Medical Genetics",

issn = "1468-6244",

publisher = "B M J PUBLISHING GROUP",

}

TY - JOUR

T1 - p63 mutations account for a range of congenital anomaly syndromes with a clear genotype phenotype correlation

AU - Brunner, H

AU - McGrath, J A

AU - Celli, J

AU - Duijf, P

AU - Gurrieri, F

AU - McKeon, F

AU - Propping, P

AU - Bamshad, M

AU - van Bokhoven, H

AU - Hamel, B

AU - Neri, G

AU - Doetsch, V

AU - de Waal, R

AU - Yang, A

AU - Vanmolkot, K

PY - 2000

Y1 - 2000

M3 - Meeting abstract

SN - 1468-6244

VL - 37

SP - S27 - S27

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

ER -