Similar articles for PMID: 9443881

Year	Number of Results
1987	1
1991	1
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1997	6
1998	9
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2000	14
2001	12
2002	4
2003	1
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2006	2
2007	5
2008	4
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2024	0

1

The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p.

Li L, Drayna D, Hu D, Hayward A, Gahagan S, Pabst H, Cowan MJ. Li L, et al. Am J Hum Genet. 1998 Jan;62(1):136-44. doi: 10.1086/301688. Am J Hum Genet. 1998. PMID: 9443881 Free PMC article.

2

A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p.

Moshous D, Li L, Chasseval R, Philippe N, Jabado N, Cowan MJ, Fischer A, de Villartay JP. Moshous D, et al. Hum Mol Genet. 2000 Mar 1;9(4):583-8. doi: 10.1093/hmg/9.4.583. Hum Mol Genet. 2000. PMID: 10699181

3

A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans.

Li L, Moshous D, Zhou Y, Wang J, Xie G, Salido E, Hu D, de Villartay JP, Cowan MJ. Li L, et al. J Immunol. 2002 Jun 15;168(12):6323-9. doi: 10.4049/jimmunol.168.12.6323. J Immunol. 2002. PMID: 12055248

4

A novel missense RAG-1 mutation results in T-B-NK+ SCID in Athabascan-speaking Dine Indians from the Canadian Northwest Territories.

Xiao Z, Yannone SM, Dunn E, Cowan MJ. Xiao Z, et al. Eur J Hum Genet. 2009 Feb;17(2):205-12. doi: 10.1038/ejhg.2008.150. Epub 2008 Aug 13. Eur J Hum Genet. 2009. PMID: 18701881 Free PMC article.

5

Bone marrow transplantation for T-B- severe combined immunodeficiency disease in Athabascan-speaking native Americans.

O'Marcaigh AS, DeSantes K, Hu D, Pabst H, Horn B, Li L, Cowan MJ. O'Marcaigh AS, et al. Bone Marrow Transplant. 2001 Apr;27(7):703-9. doi: 10.1038/sj.bmt.1702831. Bone Marrow Transplant. 2001. PMID: 11360109

6

Prenatal diagnosis and carrier detection for Athabascan severe combined immunodeficiency disease.

Li L, Zhou Y, Wang J, Hu D, Cowan MJ. Li L, et al. Prenat Diagn. 2002 Sep;22(9):763-8. doi: 10.1002/pd.400. Prenat Diagn. 2002. PMID: 12224067

7

Oral and genital ulceration: a unique presentation of immunodeficiency in Athabascan-speaking American Indian children with severe combined immunodeficiency.

Kwong PC, O'Marcaigh AS, Howard R, Cowan MJ, Frieden IJ. Kwong PC, et al. Arch Dermatol. 1999 Aug;135(8):927-31. doi: 10.1001/archderm.135.8.927. Arch Dermatol. 1999. PMID: 10456341

8

Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.

Kibar Z, Dubé MP, Powell J, McCuaïg C, Hayflick SJ, Zonana J, Hovnanian A, Radhakrishna U, Antonarakis SE, Benohanian A, Sheeran AD, Stephan ML, Gosselin R, Kelsell DP, Christianson AL, Fraser FC, Der Kaloustian VM, Rouleau GA. Kibar Z, et al. Eur J Hum Genet. 2000 May;8(5):372-80. doi: 10.1038/sj.ejhg.5200471. Eur J Hum Genet. 2000. PMID: 10854098

9

Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

Cerosaletti KM, Lange E, Stringham HM, Weemaes CM, Smeets D, Sölder B, Belohradsky BH, Taylor AM, Karnes P, Elliott A, Komatsu K, Gatti RA, Boehnke M, Concannon P. Cerosaletti KM, et al. Am J Hum Genet. 1998 Jul;63(1):125-34. doi: 10.1086/301927. Am J Hum Genet. 1998. PMID: 9634525 Free PMC article.

10

A genetic locus for adolescent idiopathic scoliosis linked to chromosome 19p13.3.

Chan V, Fong GC, Luk KD, Yip B, Lee MK, Wong MS, Lu DD, Chan TK. Chan V, et al. Am J Hum Genet. 2002 Aug;71(2):401-6. doi: 10.1086/341607. Epub 2002 Jun 28. Am J Hum Genet. 2002. PMID: 12094330 Free PMC article.

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