Houge G - Search Results

1

Array-CGH fine mapping of minor and cryptic HR-CGH detected genomic imbalances in 80 out of 590 patients with abnormal development.

Lybaek H, Meza-Zepeda LA, Kresse SH, Høysaeter T, Steen VM, Houge G. Lybaek H, et al. Among authors: houge g. Eur J Hum Genet. 2008 Nov;16(11):1318-28. doi: 10.1038/ejhg.2008.78. Epub 2008 May 7. Eur J Hum Genet. 2008. PMID: 18461090

2

Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.

Ness GO, Lybaek H, Houge G. Ness GO, et al. Among authors: houge g. Am J Med Genet. 2002 Nov 22;113(2):125-36. doi: 10.1002/ajmg.10593. Am J Med Genet. 2002. PMID: 12407702

3

Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCR.

Houge G, Liehr T, Schoumans J, Ness GO, Solland K, Starke H, Claussen U, Strømme P, Akre B, Vermeulen S. Houge G, et al. Am J Med Genet A. 2003 Apr 30;118A(3):235-40. doi: 10.1002/ajmg.a.10106. Am J Med Genet A. 2003. PMID: 12673653

4

[Diagnosis of cryptic chromosome aberrations].

Ness GO, Houge G. Ness GO, et al. Among authors: houge g. Tidsskr Nor Laegeforen. 2003 Sep 11;123(17):2418-21. Tidsskr Nor Laegeforen. 2003. PMID: 14562774 Review. Norwegian.

5

Lack of meiotic crossovers during oogenesis in an apparent 45,X Ullrich-Turner syndrome patient with three children.

Houge G, Boman H, Lybaek H, Ness GO, Juliusson PB. Houge G, et al. Am J Med Genet A. 2006 May 15;140(10):1092-7. doi: 10.1002/ajmg.a.31204. Am J Med Genet A. 2006. PMID: 16596671

6

Monosomy 8 rescue gave cells with a normal karyotype in a mildly affected man with 46,XY,r(8) mosaicism.

Gradek GA, Kvistad PH, Houge G. Gradek GA, et al. Among authors: houge g. Eur J Med Genet. 2006 Jul-Aug;49(4):292-7. doi: 10.1016/j.ejmg.2005.08.004. Epub 2005 Oct 6. Eur J Med Genet. 2006. PMID: 16829350

7

Angioma serpiginosum with oesophageal papillomatosis is an X-linked dominant condition that maps to Xp11.3-Xq12.

Blinkenberg EO, Brendehaug A, Sandvik AK, Vatne O, Hennekam RC, Houge G. Blinkenberg EO, et al. Among authors: houge g. Eur J Hum Genet. 2007 May;15(5):543-7. doi: 10.1038/sj.ejhg.5201800. Epub 2007 Mar 7. Eur J Hum Genet. 2007. PMID: 17342156

8

A 2.1 Mb deletion adjacent but distal to a 14q21q23 paracentric inversion in a family with spherocytosis and severe learning difficulties.

Lybaek H, Øyen N, Fauske L, Houge G. Lybaek H, et al. Among authors: houge g. Clin Genet. 2008 Dec;74(6):553-9. doi: 10.1111/j.1399-0004.2008.01072.x. Epub 2008 Aug 18. Clin Genet. 2008. PMID: 18717686

9

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.

Lybaek H, Ørstavik KH, Prescott T, Hovland R, Breilid H, Stansberg C, Steen VM, Houge G. Lybaek H, et al. Among authors: houge g. Eur J Hum Genet. 2009 Jul;17(7):904-10. doi: 10.1038/ejhg.2008.261. Epub 2009 Jan 21. Eur J Hum Genet. 2009. PMID: 19156171 Free PMC article.

10

Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child: a result of failed tetraploidy correction?

Houge G, Lybaek H, Gulati S. Houge G, et al. BMC Med Genet. 2009 May 18;10:42. doi: 10.1186/1471-2350-10-42. BMC Med Genet. 2009. PMID: 19445731 Free PMC article.

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