Contiguous gene deletion of MSH6 and FBXO11. Presenting a large family with Lynch syndrome and FBX011-related intellectual developmental disorder

Malene Lundsgaard; Uffe B. Jensen; Anja Ernst; Henrik Okkels; Rikke Christensen; Thomas Balslev; Lone Sunde; Charlotte K. Lautrup

Contiguous gene deletion of MSH6 and FBXO11. Presenting a large family with Lynch syndrome and FBX011-related intellectual developmental disorder

Malene Lundsgaard, Uffe B. Jensen, Anja Ernst, Henrik Okkels, Rikke Christensen, Thomas Balslev, Lone Sunde, Charlotte K. Lautrup

Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

Original language	English
Journal	European Journal of Human Genetics
Volume	30
Issue number	Suppl. 1
Pages (from-to)	237
Number of pages	1
ISSN	1018-4813
Publication status	Published - 7 Apr 2022
Event	54th European Society Human Genetics (ESHG) Conference - Virtual Duration: 28 Aug 2021 → 31 Aug 2021 https://2021.eshg.org/

Conference

Conference	54th European Society Human Genetics (ESHG) Conference
Location	Virtual
Period	28/08/2021 → 31/08/2021
Internet address	https://2021.eshg.org/

Bibliographical note

Abstract No. P08.026.D

AUB Link

Search for the material in Aalborg University Library's search engine

Cite this

@article{7f4771320ea1456cba7c0c1e760c0bca,

title = "Contiguous gene deletion of MSH6 and FBXO11. Presenting a large family with Lynch syndrome and FBX011-related intellectual developmental disorder",

author = "Malene Lundsgaard and Jensen, {Uffe B.} and Anja Ernst and Henrik Okkels and Rikke Christensen and Thomas Balslev and Lone Sunde and Lautrup, {Charlotte K.}",

note = "Abstract No. P08.026.D; 54th European Society Human Genetics (ESHG) Conference ; Conference date: 28-08-2021 Through 31-08-2021",

year = "2022",

month = apr,

day = "7",

language = "English",

volume = "30",

pages = "237",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "Suppl. 1",

url = "https://2021.eshg.org/",

}

Contiguous gene deletion of MSH6 and FBXO11. Presenting a large family with Lynch syndrome and FBX011-related intellectual developmental disorder. / Lundsgaard, Malene; Jensen, Uffe B.; Ernst, Anja et al.
In: European Journal of Human Genetics, Vol. 30, No. Suppl. 1, 07.04.2022, p. 237.

Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

TY - ABST

T1 - Contiguous gene deletion of MSH6 and FBXO11. Presenting a large family with Lynch syndrome and FBX011-related intellectual developmental disorder

AU - Lundsgaard, Malene

AU - Jensen, Uffe B.

AU - Ernst, Anja

AU - Okkels, Henrik

AU - Christensen, Rikke

AU - Balslev, Thomas

AU - Sunde, Lone

AU - Lautrup, Charlotte K.

N1 - Abstract No. P08.026.D

PY - 2022/4/7

Y1 - 2022/4/7

UR - https://www-nature-com.auh.aub.aau.dk/articles/s41431-021-01026-1

M3 - Conference abstract in journal

SN - 1018-4813

VL - 30

SP - 237

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - Suppl. 1

T2 - 54th European Society Human Genetics (ESHG) Conference

Y2 - 28 August 2021 through 31 August 2021

ER -

Contiguous gene deletion of MSH6 and FBXO11. Presenting a large family with Lynch syndrome and FBX011-related intellectual developmental disorder

Conference

Bibliographical note

AUB Link

Other files and links

Cite this