Annerén G - Search Results

1

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

2

Lowe oculocerebrorenal syndrome: DNA-based linkage of the gene to Xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosis.

Wadelius C, Fagerholm P, Pettersson U, Annerén G. Wadelius C, et al. Among authors: anneren g. Am J Hum Genet. 1989 Feb;44(2):241-7. Am J Hum Genet. 1989. PMID: 2912070 Free PMC article.

3

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

4

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.

5

Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation.

Ahlbom BE, Sidenvall R, Annerén G. Ahlbom BE, et al. Among authors: anneren g. Am J Med Genet. 1996 Aug 23;64(3):501-5. doi: 10.1002/(SICI)1096-8628(19960823)64:3<501::AID-AJMG11>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8862630

6

Genetic and linkage analysis of familial congenital hypothyroidism: exclusion of linkage to the TSH receptor gene.

Ahlbom BD, Yaqoob M, Larsson A, Ilicki A, Annerén G, Wadelius C. Ahlbom BD, et al. Among authors: anneren g. Hum Genet. 1997 Feb;99(2):186-90. doi: 10.1007/s004390050335. Hum Genet. 1997. PMID: 9048917

7

Linkage analysis excludes familial congenital hypothyroidism from chromosome 21.

Ahlbom BE, Yaqoob M, Annerén G, Larsson A, Ilicki A, Wadelius C. Ahlbom BE, et al. Among authors: anneren g. Genet Couns. 1998;9(4):265-70. Genet Couns. 1998. PMID: 9894163

8

Severe psychomotor retardation in a boy with a supernumerary derivative chromosome resulting in partial trisomy 21 and partial trisomy 7p.

Ahlbom BE, Wahlström J, Saalman R, Wadelius C, Annerén G. Ahlbom BE, et al. Among authors: anneren g. Ann Genet. 2003 Jan-Mar;46(1):29-35. doi: 10.1016/s0003-3995(03)00002-9. Ann Genet. 2003. PMID: 12818527

9

Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype.

Ahlbom BE, Goetz P, Korenberg JR, Pettersson U, Seemanova E, Wadelius C, Zech L, Annerén G. Ahlbom BE, et al. Among authors: anneren g. Am J Med Genet. 1996 Jun 28;63(4):566-72. doi: 10.1002/(SICI)1096-8628(19960628)63:4<566::AID-AJMG10>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8826436

10

Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisation.

Sillén A, Wadelius C, Annerén G. Sillén A, et al. Among authors: anneren g. Am J Med Genet. 1998 Nov 2;80(2):163-8. Am J Med Genet. 1998. PMID: 9805135

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