Search details
1.
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
Nat Genet
; 19(1): 32-8, 1998 May.
Article
in English
| MEDLINE | ID: mdl-9590285
2.
Telomere length measurement can distinguish pathogenic from non-pathogenic variants in the shelterin component, TIN2.
Clin Genet
; 81(1): 76-81, 2012 Jan.
Article
in English
| MEDLINE | ID: mdl-21199492
3.
Reduced-intensity conditioning using fludarabine and antithymocyte globulin alone allows stable engraftment in a patient with dyskeratosis congenita.
Acta Haematol
; 124(4): 200-3, 2010.
Article
in English
| MEDLINE | ID: mdl-21042011
4.
Dyskeratosis congenita: the diverse clinical presentation of mutations in the telomerase complex.
Biochimie
; 90(1): 122-30, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-17825470
5.
The molecular basis of glucose-6-phosphate dehydrogenase deficiency.
Trends Genet
; 8(4): 138-43, 1992 Apr.
Article
in English
| MEDLINE | ID: mdl-1631957
6.
A ribosome-related signature in peripheral blood CLL B cells is linked to reduced survival following treatment.
Cell Death Dis
; 7(6): e2249, 2016 06 02.
Article
in English
| MEDLINE | ID: mdl-27253413
7.
An Ashkenazi Jewish woman presenting with favism.
J Clin Pathol
; 58(3): 317-9, 2005 Mar.
Article
in English
| MEDLINE | ID: mdl-15735168
8.
Myeloid to lymphoid clonal succession following autologous transplantation in second chronic phase of chronic myeloid leukaemia.
Leukemia
; 9(12): 2138-9, 1995 Dec.
Article
in English
| MEDLINE | ID: mdl-8609730
9.
Clonal instability preceding lymphoid blastic transformation of chronic myeloid leukemia.
Leukemia
; 11(2): 195-201, 1997 Feb.
Article
in English
| MEDLINE | ID: mdl-9009080
10.
Cloning of the glucose 6-phosphate dehydrogenase gene from Plasmodium falciparum.
Mol Biochem Parasitol
; 64(2): 313-26, 1994 Apr.
Article
in English
| MEDLINE | ID: mdl-7935609
11.
Lymphoid transformation in a CML patient in complete cytogenetic remission following treatment with imatinib.
Leuk Res
; 28 Suppl 1: S75-7, 2004 May.
Article
in English
| MEDLINE | ID: mdl-15036946
12.
Non-TBI stem cell transplantation protocol for Fanconi anaemia using HLA-compatible sibling and unrelated donors.
Bone Marrow Transplant
; 32(7): 653-6, 2003 Oct.
Article
in English
| MEDLINE | ID: mdl-13130311
13.
DNA Genotypic Conservation During Phenotypic Switch from T-cell Acute Lymphoblastic Leukaemia to Acute Myeloblastic Leukaemia.
Leuk Lymphoma
; 1(1): 21-8, 1989.
Article
in English
| MEDLINE | ID: mdl-27456403
14.
Tetanus toxin: a marker of amphibian neuronal differentiation in vitro.
Neurosci Lett
; 22(2): 87-90, 1981 Mar 10.
Article
in English
| MEDLINE | ID: mdl-7015184
15.
An atypical form of dyskeratosis congenita with renal agenesis and no mutation in DKC1, TERC and TERT genes.
J Eur Acad Dermatol Venereol
; 23(5): 607-8, 2009 May.
Article
in English
| MEDLINE | ID: mdl-19415813
16.
Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia.
Leukemia
; 30(10): 2083-2086, 2016 10.
Article
in English
| MEDLINE | ID: mdl-27133828
17.
Primary Ki-1 lymphoma and the aetiology of B symptoms.
Eur J Cancer
; 32A(5): 902-3, 1996 May.
Article
in English
| MEDLINE | ID: mdl-9081378
18.
A T cell clone in association with an Epstein-Barr virus-related B cell lymphoma.
Transplantation
; 52(6): 1108-9, 1991 Dec.
Article
in English
| MEDLINE | ID: mdl-1661038
19.
Factor V Leiden and sickle cell disease.
Thromb Haemost
; 75(5): 859-60, 1996 May.
Article
in English
| MEDLINE | ID: mdl-8725738
20.
The 20210A allele of prothrombin is not found among sickle cell disease patients from West Africa.
Thromb Haemost
; 79(2): 444-5, 1998 Feb.
Article
in English
| MEDLINE | ID: mdl-9493606