X-linked Wiskott-Aldrich syndrome in a girl

[1] ALLEN RC, 1992, AM J HUM GENET, V51, P1229

[2] Aral B, 1996, HUM MUTAT, V7, P52, DOI 10.1002/(SICI)1098-1004(1996)7:1<52::AID-HUMU7>3.3.CO

[3] 2-0

[4] X-CHROMOSOME METHYLATION IN MANIFESTING AND HEALTHY CARRIERS OF DYSTROPHINOPATHIES - CONCORDANCE OF ACTIVATION RATIOS AMONG FIRST DEGREE FEMALE RELATIVES AND SKEWED INACTIVATION AS CAUSE OF THE AFFECTED PHENOTYPES [J]. HUMAN GENETICS, 1995, 96 (02) : 167 - 176

[5] Belmont JW, 1996, AM J HUM GENET, V58, P1101

[6] CLARKE JTR, 1991, AM J HUM GENET, V49, P289

[7] CONLEY ME, 1992, BLOOD, V80, P1264

[8] DERRY JM, 1994, CELL, V79, pA922

[9] ISOLATION OF A NOVEL GENE MUTATED IN WISKOTT-ALDRICH SYNDROME [J]. CELL, 1994, 78 (04) : 635 - 644

[10] FEARON ER, 1988, BLOOD, V72, P1735

[1] ALLEN RC, 1992, AM J HUM GENET, V51, P1229

[2] Aral B, 1996, HUM MUTAT, V7, P52, DOI 10.1002/(SICI)1098-1004(1996)7:1<52::AID-HUMU7>3.3.CO

[3] 2-0

[4] X-CHROMOSOME METHYLATION IN MANIFESTING AND HEALTHY CARRIERS OF DYSTROPHINOPATHIES - CONCORDANCE OF ACTIVATION RATIOS AMONG FIRST DEGREE FEMALE RELATIVES AND SKEWED INACTIVATION AS CAUSE OF THE AFFECTED PHENOTYPES [J]. HUMAN GENETICS, 1995, 96 (02) : 167 - 176

[5] Belmont JW, 1996, AM J HUM GENET, V58, P1101

[6] CLARKE JTR, 1991, AM J HUM GENET, V49, P289

[7] CONLEY ME, 1992, BLOOD, V80, P1264

[8] DERRY JM, 1994, CELL, V79, pA922

[9] ISOLATION OF A NOVEL GENE MUTATED IN WISKOTT-ALDRICH SYNDROME [J]. CELL, 1994, 78 (04) : 635 - 644

[10] FEARON ER, 1988, BLOOD, V72, P1735