-
1
-
-
0001102239
-
Pedigree demonstrating a sex-linked recessive condition characterised by draining ears, eczematoid dermatitis and bloody diarrhoea
-
Aldrich R.A., Steinberg A.G. & Campbell D.C. (1954) Pedigree demonstrating a sex-linked recessive condition characterised by draining ears, eczematoid dermatitis and bloody diarrhoea. Paediatrics 13, 133-139.
-
(1954)
Paediatrics
, vol.13
, pp. 133-139
-
-
Aldrich, R.A.1
Steinberg, A.G.2
Campbell, D.C.3
-
2
-
-
0028880534
-
Scanning of the Wiskott-Aldrich syndrome (WAS) gene: Identification of 18 novel alterations including a possible mutation hotspot at Arg86 resulting in thrombocytopenia, a mild WAS phenotype
-
Kwan S.P., Hagemann T.L., Blaese R.M., Knutsen A. & Rosen F.S. (1995) Scanning of the Wiskott-Aldrich syndrome (WAS) gene: identification of 18 novel alterations including a possible mutation hotspot at Arg86 resulting in thrombocytopenia, a mild WAS phenotype. Human Molecular Genetics 4, 1995-1998.
-
(1995)
Human Molecular Genetics
, vol.4
, pp. 1995-1998
-
-
Kwan, S.P.1
Hagemann, T.L.2
Blaese, R.M.3
Knutsen, A.4
Rosen, F.S.5
-
3
-
-
0016199048
-
X-linked idiopathic thrombocytopenia
-
Moore J.R. (1974) X-linked idiopathic thrombocytopenia. Clinical Genetics 5, 344-350.
-
(1974)
Clinical Genetics
, vol.5
, pp. 344-350
-
-
Moore, J.R.1
-
4
-
-
0029836850
-
Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein gene
-
de Saint Basile G., Lagelouse R.D., Lambert N. et al. (1996) Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein gene. Journal of Paediatrics 129, 56-62.
-
(1996)
Journal of Paediatrics
, vol.129
, pp. 56-62
-
-
De Saint Basile, G.1
Lagelouse, R.D.2
Lambert, N.3
-
5
-
-
0008893043
-
Familial idiopathic thrombocytopenic purpura
-
Schaar F.E. (1963) Familial idiopathic thrombocytopenic purpura. Journal of Paediatrics 62, 546-551.
-
(1963)
Journal of Paediatrics
, vol.62
, pp. 546-551
-
-
Schaar, F.E.1
-
6
-
-
9244222658
-
Mutation spectrum in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia: Identification of twelve different mutations in the WASP gene
-
Schwarz M., Bekassy A., Donner M. et al. (1996) Mutation spectrum in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia: identification of twelve different mutations in the WASP gene. Thrombosis and Haemostasis 75, 546-550.
-
(1996)
Thrombosis and Haemostasis
, vol.75
, pp. 546-550
-
-
Schwarz, M.1
Bekassy, A.2
Donner, M.3
-
7
-
-
0000788042
-
Familiarer, angeborener Morbus Werlhofii?
-
Wiskott A.L. (1937) Familiarer, angeborener Morbus Werlhofii? Monatsschr Kinderheilkd 68, 212-216.
-
(1937)
Monatsschr Kinderheilkd
, vol.68
, pp. 212-216
-
-
Wiskott, A.L.1
-
8
-
-
0030804315
-
Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype
-
Zhu Q., Watanabe C., Liu T. et al. (1997) Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype. Blood 90, 2680-2689.
-
(1997)
Blood
, vol.90
, pp. 2680-2689
-
-
Zhu, Q.1
Watanabe, C.2
Liu, T.3
-
9
-
-
0028786330
-
The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene
-
Zhu Q., Zhang M., Blaese R.M. et al. (1995) The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene. Blood 86, 3797-3804.
-
(1995)
Blood
, vol.86
, pp. 3797-3804
-
-
Zhu, Q.1
Zhang, M.2
Blaese, R.M.3
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