Familial Multiple Lipomatosis - analyses of genetic etiology by whole genome sequencing and delineation of the clinical phenotype

Julie Bjerrelund; Martin J. Larsen; Henrik D. Schrøder; Morten Frost; Moustapha Kassem; Lilian B. Ousager; Anja L. Frederiksen

Familial Multiple Lipomatosis - analyses of genetic etiology by whole genome sequencing and delineation of the clinical phenotype

Julie Bjerrelund, Martin J. Larsen, Henrik D. Schrøder, Morten Frost, Moustapha Kassem, Lilian B. Ousager, Anja L. Frederiksen

Publikation: Bidrag til tidsskrift › Konferenceabstrakt i tidsskrift › Forskning › peer review

Originalsprog	Engelsk
Tidsskrift	European Journal of Human Genetics
Vol/bind	30
Udgave nummer	Suppl. 1
Sider (fra-til)	205
Antal sider	1
ISSN	1018-4813
Status	Udgivet - 7 apr. 2022
Begivenhed	54th European Society Human Genetics (ESHG) Conference - Virtual Varighed: 28 aug. 2021 → 31 aug. 2021 https://2021.eshg.org/

Konference

Konference	54th European Society Human Genetics (ESHG) Conference
Lokation	Virtual
Periode	28/08/2021 → 31/08/2021
Internetadresse	https://2021.eshg.org/

Bibliografisk note

Abstrakt No. P06.014.C

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Citationsformater

@article{dcefa044262f4669a1ce50815bb25fef,

title = "Familial Multiple Lipomatosis - analyses of genetic etiology by whole genome sequencing and delineation of the clinical phenotype",

author = "Julie Bjerrelund and Larsen, {Martin J.} and Schr{\o}der, {Henrik D.} and Morten Frost and Moustapha Kassem and Ousager, {Lilian B.} and Frederiksen, {Anja L.}",

note = "Abstract No. P06.014.C; 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 = "205",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

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}

Familial Multiple Lipomatosis - analyses of genetic etiology by whole genome sequencing and delineation of the clinical phenotype. / Bjerrelund, Julie; Larsen, Martin J.; Schrøder, Henrik D. et al.
I: European Journal of Human Genetics, Bind 30, Nr. Suppl. 1, 07.04.2022, s. 205.

Publikation: Bidrag til tidsskrift › Konferenceabstrakt i tidsskrift › Forskning › peer review

TY - ABST

T1 - Familial Multiple Lipomatosis - analyses of genetic etiology by whole genome sequencing and delineation of the clinical phenotype

AU - Bjerrelund, Julie

AU - Larsen, Martin J.

AU - Schrøder, Henrik D.

AU - Frost, Morten

AU - Kassem, Moustapha

AU - Ousager, Lilian B.

AU - Frederiksen, Anja L.

N1 - Abstract No. P06.014.C

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 - 205

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 -