Ehlers Danlos syndrome, kyphoscoliotic type due to Lysyl Hydroxylase 1 deficiency in two children without congenital or early onset kyphoscoliosis

FS van Dijk; Grazia Verheijen - Mancini; A Maugeri; JM Cobben

doi:10.1016/j.ejmg.2017.07.011

Ehlers Danlos syndrome, kyphoscoliotic type due to Lysyl Hydroxylase 1 deficiency in two children without congenital or early onset kyphoscoliosis

FS van Dijk
, Grazia Verheijen - Mancini
, A Maugeri
, JM Cobben

Clinical Genetics

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

10 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	536-540
Number of pages	5
Journal	European Journal of Medical Genetics
Volume	60
Issue number	10
DOIs	https://doi.org/10.1016/j.ejmg.2017.07.011
Publication status	Published - 2017

Research programs

EMC OR-01

Access to Document

10.1016/j.ejmg.2017.07.011

http://hdl.handle.net/1765/101650

Cite this

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title = "Ehlers Danlos syndrome, kyphoscoliotic type due to Lysyl Hydroxylase 1 deficiency in two children without congenital or early onset kyphoscoliosis",

author = "\{van Dijk\}, FS and \{Verheijen - Mancini\}, Grazia and A Maugeri and JM Cobben",

year = "2017",

doi = "10.1016/j.ejmg.2017.07.011",

language = "Undefined/Unknown",

volume = "60",

pages = "536--540",

journal = "European Journal of Medical Genetics",

issn = "1769-7212",

publisher = "Elsevier Masson",

number = "10",

}

TY - JOUR

T1 - Ehlers Danlos syndrome, kyphoscoliotic type due to Lysyl Hydroxylase 1 deficiency in two children without congenital or early onset kyphoscoliosis

AU - van Dijk, FS

AU - Verheijen - Mancini, Grazia

AU - Maugeri, A

AU - Cobben, JM

PY - 2017

Y1 - 2017

U2 - 10.1016/j.ejmg.2017.07.011

DO - 10.1016/j.ejmg.2017.07.011

M3 - Article

C2 - 28757364

SN - 1769-7212

VL - 60

SP - 536

EP - 540

JO - European Journal of Medical Genetics

JF - European Journal of Medical Genetics

IS - 10

ER -