Publications by authors named "Jennifer Skaug"

Claim this Profile
S
Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug

Am J Hum Genet· February 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Contribution of SHANK3 mutations to autism spectrum disorder.
Rainald Moessner, Christian R Marshall, James S Sutcliffe, Jennifer Skaug, Dalila Pinto

Am J Hum Genet· December 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Nat Genet· March 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.
Lars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, Jennifer Skaug, Kazuhiko Nakabayashi

Am J Hum Genet· November 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular basis for expression of common and rare fragile sites.
Eitan Zlotorynski, Ayelet Rahat, Jennifer Skaug, Neta Ben-Porat, Efrat Ozeri

Mol Cell Biol· October 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human chromosome 7: DNA sequence and biology.
Stephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, Lucy R Osborne, Kazuhiko Nakabayashi, Jennifer Skaug

Science· May 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans.
Xiao-Yan Wen, Robert A Hegele, Jian Wang, Ding Yan Wang, Joseph Cheung, Jennifer Skaug

Hum Mol Genet· May 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5).
Anne-Marie Lamhonwah, Jennifer Skaug, Stephen W Scherer, Ingrid Tein

Biochem Biophys Res Commun· January 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis