Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia‐derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 …
S Meyer, WD Fergusson, AD Whetton… - Genes …, 2007 - Wiley Online Library
Fanconi anemia (FA) is an inherited disease with congenital abnormalities and an extreme
risk of acute myeloid leukemia (AML). Genetic events occurring during malignant …
risk of acute myeloid leukemia (AML). Genetic events occurring during malignant …
A cross‐linker‐sensitive myeloid leukemia cell line from a 2‐year‐old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations
S Meyer, WD Fergusson, AB Oostra… - Genes …, 2005 - Wiley Online Library
Fanconi anemia (FA) is a rare autosomal recessive disorder characterized by congenital
and developmental abnormalities, hypersensitivity to DNA cross‐linking agents such as …
and developmental abnormalities, hypersensitivity to DNA cross‐linking agents such as …
X linked lymphoproliferative disease in a United Kingdom family
PD Arkwright, G Makin, AM Will, M Ayres… - Archives of disease in …, 1998 - adc.bmj.com
X linked lymphoproliferative disease (XLP; Duncan's disease) is a rare disorder affecting
boys and characterised by a defective immune response to Epstein-Barr virus caused by a …
boys and characterised by a defective immune response to Epstein-Barr virus caused by a …
[HTML][HTML] Amino acid transport systems β and A in fetal T lymphocytes in intrauterine growth restriction and with tumor necrosis factor-α treatment
CG Iruloh, SW D'Souza, WD Fergusson, PN Baker… - Pediatric …, 2009 - nature.com
Intrauterine growth restriction (IUGR) is associated with reduced activity of placental amino
acid transport systems β and A. Whether this phenotype is maintained in fetal cells outside …
acid transport systems β and A. Whether this phenotype is maintained in fetal cells outside …
[CITATION][C] LIM–kinase deleted in Williams syndrome
M Tassabehji, K Metcalfe, WD Fergusson… - Nature …, 1996 - nature.com
Sir-Williams syndrome (WS) is believed to be a contiguous gene syndrome caused by
deletion of elastin and of other unknown genes1• 2 on chromosome 7. WS is generally …
deletion of elastin and of other unknown genes1• 2 on chromosome 7. WS is generally …
Infantile osteopetrosis; bone marrow transplantation from a cousin donor.
GM Taylor, SP Dearden, AM Will, DI Evans… - Archives of disease in …, 1995 - adc.bmj.com
The successful correction of infantile osteopetrosis in an Asian child by bone marrow
transplantation (BMT) from an HLA-A, B matched cousin donor is reported. Retrospective …
transplantation (BMT) from an HLA-A, B matched cousin donor is reported. Retrospective …