Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome

S Schiller; S Spranger; B Schechinger; M Fukami; S Merker; Sten Drop; J Tröger; H Knoblauch; J Kunze; J Seidel; GA Rappold

doi:10.1038/sj.ejhg.5200402

Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome

S Schiller, S Spranger, B Schechinger, M Fukami, S Merker, Sten Drop, J Tröger, H Knoblauch, J Kunze, J Seidel, GA Rappold

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

134 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	54-62
Number of pages	9
Journal	European Journal of Human Genetics
Volume	8
DOIs	https://doi.org/10.1038/sj.ejhg.5200402
Publication status	Published - 2000
Externally published	Yes

Research programs

EMC MM-01-54-01

Access to Document

10.1038/sj.ejhg.5200402

http://hdl.handle.net/1765/64224

Cite this

@article{a019b5cd07e443868917cdd8d5a61707,

title = "Phenotypic variation and genetic heterogeneity in L{\'e}ri-Weill syndrome",

author = "S Schiller and S Spranger and B Schechinger and M Fukami and S Merker and Sten Drop and J Tr{\"o}ger and H Knoblauch and J Kunze and J Seidel and GA Rappold",

year = "2000",

doi = "10.1038/sj.ejhg.5200402",

language = "Undefined/Unknown",

volume = "8",

pages = "54--62",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer Nature",

}

TY - JOUR

T1 - Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome

AU - Schiller, S

AU - Spranger, S

AU - Schechinger, B

AU - Fukami, M

AU - Merker, S

AU - Drop, Sten

AU - Tröger, J

AU - Knoblauch, H

AU - Kunze, J

AU - Seidel, J

AU - Rappold, GA

PY - 2000

Y1 - 2000

U2 - 10.1038/sj.ejhg.5200402

DO - 10.1038/sj.ejhg.5200402

M3 - Article

SN - 1018-4813

VL - 8

SP - 54

EP - 62

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

ER -