Annerén G - Search Results

1

Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia.

Tentler D, Gustavsson P, Leisti J, Schueler M, Chelly J, Timonen E, Annerén G, Willard HF, Dahl N. Tentler D, et al. Among authors: anneren g. Eur J Hum Genet. 1999 Jul;7(5):541-8. doi: 10.1038/sj.ejhg.5200320. Eur J Hum Genet. 1999. PMID: 10439959

2

Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism.

Ahlbom BE, Yaqoob M, Gustavsson P, Abbas HG, Annerén G, Larsson A, Wadelius C. Ahlbom BE, et al. Among authors: anneren g. Hum Genet. 2002 Feb;110(2):145-7. doi: 10.1007/s00439-002-0680-z. Epub 2002 Jan 29. Hum Genet. 2002. PMID: 11935320

3

Klar J, Asling B, Carlsson B, Ulvsbäck M, Dellsén A, Ström C, Rhedin M, Forslund A, Annerén G, Ludvigsson JF, Dahl N. Klar J, et al. Among authors: anneren g. Eur J Hum Genet. 2005 Aug;13(8):928-34. doi: 10.1038/sj.ejhg.5201433. Eur J Hum Genet. 2005. PMID: 15886715

4

Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus.

Ahlbom BE, Dahl N, Zetterqvist P, Annerén G. Ahlbom BE, et al. Among authors: anneren g. Clin Genet. 1995 Aug;48(2):85-9. doi: 10.1111/j.1399-0004.1995.tb04061.x. Clin Genet. 1995. PMID: 7586657

5

Linkage mapping of a severe X-linked mental retardation syndrome.

Malmgren H, Sundvall M, Dahl N, Gustavson KH, Annerén G, Wadelius C, Steén-Bondeson ML, Pettersson U. Malmgren H, et al. Among authors: anneren g. Am J Hum Genet. 1993 Jun;52(6):1046-52. Am J Hum Genet. 1993. PMID: 8503440 Free PMC article.

6

Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22.

Arnell H, Nemeth A, Annerén G, Dahl N. Arnell H, et al. Among authors: anneren g. Hum Genet. 1997 Sep;100(3-4):378-81. doi: 10.1007/s004390050519. Hum Genet. 1997. PMID: 9272158

7

Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3).

Gustavsson P, Kimber E, Wahlström J, Annerén G. Gustavsson P, et al. Among authors: anneren g. Am J Med Genet. 1999 Feb 12;82(4):348-51. Am J Med Genet. 1999. PMID: 10051171

8

A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint.

Tentler D, Brandberg G, Betancur C, Gillberg C, Annerén G, Orsmark C, Green ED, Carlsson B, Dahl N. Tentler D, et al. Among authors: anneren g. Am J Med Genet. 2001 Dec 8;105(8):729-36. doi: 10.1002/ajmg.1607. Am J Med Genet. 2001. PMID: 11803521 Free article.

9

Molecular genetic analysis of a de novo balanced translocation t(6;17)(p21.31;q11.2) associated with hypospadias and anorectal malformation.

Mansouri MR, Carlsson B, Davey E, Nordenskjöld A, Wester T, Annerén G, Läckgren G, Dahl N. Mansouri MR, et al. Among authors: anneren g. Hum Genet. 2006 Mar;119(1-2):162-8. doi: 10.1007/s00439-005-0122-9. Epub 2006 Jan 3. Hum Genet. 2006. PMID: 16395596

10

Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida.

Gustavsson P, Schoumans J, Staaf J, Borg A, Nordenskjöld M, Annerén G. Gustavsson P, et al. Among authors: anneren g. Eur J Med Genet. 2007 May-Jun;50(3):237-41. doi: 10.1016/j.ejmg.2007.01.004. Epub 2007 Feb 21. Eur J Med Genet. 2007. PMID: 17387046

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