Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome

M Kalff-Suske, A Wild, M.G.E.M. Ausems, X et al.

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

Keywords

@article{7b404be8eea74dea84bb516ea164f154,

title = "Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome",

keywords = "Econometric and Statistical Methods: General, Genetics, Geneeskunde(GENK), Overig medisch onderzoek",

author = "M Kalff-Suske and A Wild and M.G.E.M. Ausems and {et al.}, X",

year = "1999",

language = "Undefined/Unknown",

volume = "8",

pages = "1769--1777",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "9",

}

TY - JOUR

T1 - Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome

AU - Kalff-Suske, M

AU - Wild, A

AU - Ausems, M.G.E.M.

AU - et al., X

PY - 1999

Y1 - 1999

KW - Econometric and Statistical Methods: General

KW - Genetics

KW - Geneeskunde(GENK)

KW - Overig medisch onderzoek

M3 - Article

SN - 0964-6906

VL - 8

SP - 1769

EP - 1777

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 9

ER -