Search Results

Compound haplotypes at Xp11.23 and human population growth in Eurasia

Authors: S. Alonso; J. A. L. Armour

Source: Annals of Human Genetics, Volume 68, Number 5, September 2004 , pp. 428-437(10)

Publisher: Blackwell Publishing

Deletion of the factor IX gene as a result of translocation t(X;1) in a girl affected by haemophilia B

Authors: Krepischi-Santos, A. C. V.; Carneiro, J. D. A.; Svartman, M.; Bendit, I.; Odone-Filho, V.; Vianna-Morgante, A. M.

Source: British Journal of Haematology, Volume 113, Number 3, June 2001 , pp. 616-620(5)

Publisher: Blackwell Publishing

Unique and Recurrent WAS Gene Mutations in Wiskott-Aldrich Syndrome and X-Linked Thrombocytopenia

Authors: Thompson L.J.; Lalloz M.R.A.; Layton D.M.

Source: Blood Cells, Molecules, and Diseases, Volume 25, Number 4, August 1999 , pp. 218-226(9)

Publisher: Elsevier

Unique and Recurrent WAS Gene Mutations in Wiskott-Aldrich Syndrome and X-Linked Thrombocytopenia

Authors: Thompson L.J.; Lalloz M.R.A.; Weatherall D.S.D.M.

Source: Blood Cells, Molecules, and Diseases, Volume 25, Number 4, August 1999 , pp. 218-226(9)

Publisher: Academic Press

Hypermethylation of the M27β (DXS255) locus in chronic B-cell leukaemia

Authors: Crossen, Peter E.; Morrison, Mary J.

Source: British Journal of Haematology, Volume 100, Number 1, January 1998 , pp. 191-193(3)

Publisher: Blackwell Publishing

Construction of a 1.5-Mb Bacterial Artificial Chromosome Contig in Xp11.23, a Region of High Gene Content

Authors: Boycott K.M.; Zahorchak R.J.; Summer C.G.; Boycott N.P.; Kotak V.; Russell C.G.; Bech-Hansen N.T.

Source: Genomics, Volume 48, Number 3, 15 March 1998 , pp. 369-372(4)

Publisher: Elsevier

Construction of a 1.5-Mb Bacterial Artificial Chromosome Contig in Xp11.23, a Region of High Gene Content

Authors: Boycott K.M.; Zahorchak R.J.; Summer C.G.; Boycott N.P.; Kotak V.; Russell C.G.; Bech-Hansen N.T.

Source: Genomics, Volume 48, Number 3, March 1998 , pp. 369-372(4)

Publisher: Academic Press

Clonality in hematopoietic disorders

Authors: Agnew A.; Forrester P.; Hassard J.; Procter S.; Hotta T.

Source: International Journal of Hematology, Volume 66, Number 4, December 1997 , pp. 403-412(10)

Publisher: Elsevier

Confining the breakpoint regions for the papillary renal cell carcinoma-associated t(X;1) (p11;q21)

Authors: Weterman M.; Wilbrink M.; de Jong B.; van Kessel A.G.

Source: Cancer Genetics and Cytogenetics, Volume 91, Number 2, 15 October 1996 , pp. 138-138(1)

Publisher: Elsevier

A 2-Megabase Physical Contig Incorporating 43 DNA Markers on the Human X Chromosome at p11.23-p11.22 from ZNF21 to DXS255

Authors: Boycott K.M.; Halley G.R.; Schlessinger D.; Bech-Hansen N.T.

Source: Genomics, Volume 33, Number 3, May 1996 , pp. 488-497(10)

Publisher: Academic Press

Construction of Two YAC Contigs in Human Xp11.23-p11.22, One Encompassing the Loci OATL1,GATA,TFE3, and SYP, the Other Linking DXS255 to DXS146

Authors: F ISHER S.I.E.; H ATCHWELL E.L.; C HAND A.A.; O CKENDEN N.A.; M ONACO A.N.P.; C RAIG I.A.W.

Source: Genomics, Volume 29, Number 2, September 1995 , pp. 496-502(7)

Publisher: Academic Press