Annerén G - Search Results

1

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.

Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, Grigoriadou M, Albrecht B, Passarge E, Annerén G, Blennow E, Clausen N, Galla-Voumvouraki A, Tsezou A, Kitsiou-Tzeli S, Hahnemann JM, Hertz JM, Houge G, Kuklík M, Macek M, Lacombe D, Miller K, Moncla A, López Pajares I, Patsalis PC, Petersen MB, et al. Karadima G, et al. Among authors: anneren g. Eur J Hum Genet. 1998 Sep-Oct;6(5):432-8. doi: 10.1038/sj.ejhg.5200212. Eur J Hum Genet. 1998. PMID: 9801867

2

Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

Blennow E, Annerén G, Bui TH, Berggren E, Asadi E, Nordenskjöld M. Blennow E, et al. Among authors: anneren g. Am J Hum Genet. 1993 Aug;53(2):433-42. Am J Hum Genet. 1993. PMID: 8328459 Free PMC article.

3

FISH-mapping of a 100-kb terminal 22q13 deletion.

Anderlid BM, Schoumans J, Annerén G, Tapia-Paez I, Dumanski J, Blennow E, Nordenskjöld M. Anderlid BM, et al. Among authors: anneren g. Hum Genet. 2002 May;110(5):439-43. doi: 10.1007/s00439-002-0713-7. Epub 2002 Apr 4. Hum Genet. 2002. PMID: 12073014

4

An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.

Annerén G, Andersson M, Page DC, Brown LG, Berg M, Läckgren G, Gustavson KH, de la Chapelle A. Annerén G, et al. Am J Hum Genet. 1987 Oct;41(4):594-604. Am J Hum Genet. 1987. PMID: 2889356 Free PMC article.

5

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization.

Blennow E, Bui TH, Kristoffersson U, Vujic M, Annerén G, Holmberg E, Nordenskjöld M. Blennow E, et al. Among authors: anneren g. Prenat Diagn. 1994 Nov;14(11):1019-28. doi: 10.1002/pd.1970141103. Prenat Diagn. 1994. PMID: 7877949

6

Gamma-glutamyl transferase activity in the amniotic fluid of fetuses with chromosomal aberrations and inborn errors of metabolism.

Macek M, Annerén G, Gustavson KH, Held K, Tomásová H, Hronková J, Burjanková J, Hrycejová I. Macek M, et al. Among authors: anneren g. Clin Genet. 1987 Dec;32(6):403-8. doi: 10.1111/j.1399-0004.1987.tb03158.x. Clin Genet. 1987. PMID: 2893674

7

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

8

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

9

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

10

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

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