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1 . Academic Journal
Chromosomal imbalances in a recurrent solitary fibrous tumor of the orbit
저자
by
Ness, Gro Oddveig
;
Lybæk, Helle
;
Arnes, Jarle
;
Rødahl, Eyvind
.
소스
In
Cancer Genetics and Cytogenetics
2005 162(1):38-44
Full Text (ScienceDirect)
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6 . Academic Journal
LRFN5 locus structure is associated with autism and influenced by the sex of the individual and locus conversions.
저자
by
Lybæk, Helle
;
Robson, Michael
;
de Leeuw, Nicole
;
Hehir‐Kwa, Jayne Y.
;
Jeffries, Aaron
, et al.
소스
Autism Research: Official Journal of the International Society for Autism Research; Mar2022, Vol. 15 Issue 3, p421-433, 13p
Web of Science
Scopus
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7 . Academic Journal
RevSex duplication-induced and sex-related differences in the SOX9 regulatory region chromatin landscape in human fibroblasts.
저자
by
Lybæk, Helle
;
derik de Bruijn, Die
;
den Engelsman-van Dijk, Anke H. A.
;
Vanichkina, Darya
;
Nepal, Chirag
, et al.
소스
Epigenetics
. Mar2014, Vol. 9 Issue 3, p416-427. 12p.
Web of Science
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7 . Academic Journal
DCLK1 Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder.
저자
by
Håvik, Bjarte
;
Degenhardt, Franziska A.
;
Johansson, Stefan
;
Fernandes, Carla P. D.
;
Hinney, Anke
, et al.
소스
PLoS ONE
. Apr2012, Vol. 7 Issue 4, p1-12. 12p.
Web of Science
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7 . Academic Journal
The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia
저자
by
Håvik, Bjarte
;
Le Hellard, Stephanie
;
Rietschel, Marcella
;
Lybæk, Helle
;
Djurovic, Srdjan
, et al.
소스
Biological Psychiatry
. Jul2011, Vol. 70 Issue 1, p35-42. 8p.
Full Text (ScienceDirect)
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7 . Academic Journal
A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis.
저자
by
Griswold, Anthony J.
;
Ma, Deqiong
;
Sacharow, Stephanie J.
;
Robinson, Joycelyn L.
;
Jaworski, James M.
, et al.
소스
Autism Research: Official Journal of the International Society for Autism Research; Jun2011, Vol. 4 Issue 3, p221-227, 7p
Web of Science
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7 . Academic Journal
An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion.
저자
by
Lybæk, Helle
;
ørstavik, Karen Helene
;
Prescott, Trine
;
Hovland, Randi
;
Breilid, Harald
, et al.
소스
European Journal of Human Genetics
. Jul2009, Vol. 17 Issue 7, p904-910. 7p. 1 Color Photograph, 2 Diagrams, 1 Graph.
Web of Science
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7 . Academic Journal
Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child: A result of failed tetraploidy correction?
저자
by
Houge, Gunnar
;
Lybæk, Helle
;
Gulati, Sasha
.
소스
BMC Medical Genetics
. 2009, Vol. 10, Special section p1-7. 7p. 2 Color Photographs, 1 Diagram, 2 Charts.
Open Access (BioMed Central)
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5 . Academic Journal
Array-CGH fine mapping of minor and cryptic HR-CGH detected genomic imbalances in 80 out of 590 patients with abnormal development.
저자
by
Lybæk, Helle
;
Meza-Zepeda, Leonardo A.
;
Kresse, Stine H.
;
Høysæter, Trude
;
Steen, Vidar M.
, et al.
소스
European Journal of Human Genetics
. Nov2008, Vol. 16 Issue 11, p1318-1328. 11p. 2 Diagrams, 3 Charts, 1 Graph.
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7 . Academic Journal
Inheritance of a Terminal 7.1 Mb 18p Deletion Flanked by a 2.3 Mb Duplication From a Physically Normal Mother
저자
by
Misceo, Doriana
;
rstavik, Karen Helene
;
Lybæk, Helle
;
Sandvig, Inger
;
Ormerod, Eli
, et al.
소스
American Journal Of Medical Genetics - A
. Dec 01, 2009 149A(12):2877-2881
Web of Science
Scopus
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