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100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report

The New England journal of medicine, 2021-11, Vol.385 (20), p.1868-1880

2021

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Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

Lancet neurology, 2022-03, Vol.21 (3), p.234-245

2022

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Identification of novel regions of amplification and deletion within mantle cell lymphoma DNA by comparative genomic hybridization

British journal of haematology, 2002-02, Vol.116 (2), p.291-298

2002

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Mutational analysis of class III receptor tyrosine kinases (C‐KIT, C‐FMS, FLT3) in idiopathic myelofibrosis

British journal of haematology, 2003-02, Vol.120 (3), p.464-470

2003

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Identifying functionally important aberrations of Neurofibromin-1 (NF1) in non-small cell lung cancer (NSCLC)

European journal of surgical oncology, 2018-03, Vol.44, p.S36-S36

2018

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Identifying functionally important aberrations of Neurofibromin-1 (NF1) in non-small cell lung cancer (NSCLC)

European journal of surgical oncology, 2017-11, Vol.43 (11), p.2233-2233

2017

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Guidelines for the measurement of BCR‐ABL1 transcripts in chronic myeloid leukaemia

British journal of haematology, 2011-04, Vol.153 (2), p.179-190

2011

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Genetic testing in the assessment of living related kidney donors at risk of autosomal dominant polycystic kidney disease

Transplantation, 2015-05, Vol.99 (5), p.1023

2015

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Unraveling the role of C. difficile S-layer in infection and disease

Access microbiology, 2019-03, Vol.1 (1A)

2019

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Lineage‐specific chimerism monitoring after allogeneic haematopoietic stem cell transplantation: do we really know what we are measuring?

British journal of haematology, 2017-01, Vol.176 (1), p.139-141

2017

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Predicting persistent inflammatory arthritis amongst early arthritis clinic patients in the UK: is musculoskeletal ultrasound required?

Arthritis research & therapy, 2013-01, Vol.15 (5), p.R118-R118

2013

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FLT3 internal tandem duplication mutations are rare in agnogenic myeloid metaplasia

Blood, 2002-07, Vol.100 (1), p.364-364

2002

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c‐kit proto‐oncogene exon 8 in‐frame deletion plus insertion mutations in acute myeloid leukaemia

British journal of haematology, 1999-06, Vol.105 (4), p.894-900

1999

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Long term lympho-haematopoietic reconstitution by umbilical cord blood stem cells following primary graft failure and autologous rescue

British journal of haematology, 2012-08, Vol.158 (3), p.419-420

2012

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Long‐term dual donor derived haematopoietic reconstitution following double unrelated cord blood transplantation – single unit dominance is not always the case

British journal of haematology, 2010-04, Vol.149 (2), p.298-299

2010

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Early indication of emergence from vegetative state derived from assessments with the SMART-a preliminary report

Brain injury, 2000-04, Vol.14 (4), p.319-331

2000

Volltextzugriff (PDF)

Guidelines for the measurement of BCRaABL1 transcripts in chronic myeloid leukaemia

British journal of haematology, 2011-04, Vol.153 (2), p.179-190

2011

Volltextzugriff (PDF)

Late Relapsing Childhood Lymphoblastic Leukemia

Blood, 1998-10, Vol.92 (7), p.2334-2337

1998

Volltextzugriff (PDF)

Late relapsing childhood lymphoblastic leukemia

Blood, 1998-10, Vol.92 (7), p.2334-2337

1998

Volltextzugriff (PDF)

BCR-ABL transcript with an e19a2 (c3a2) junction in classical chronic myeloid leukemia

Blood, 1997-04, Vol.89 (8), p.3064-3064

1997

Volltextzugriff (PDF)

HYSTERIA AND THE WORKMEN'S COMPENSATION ACT

The Lancet (British edition), 1929-04, Vol.213 (5512), p.811-814

Wilson Gill, A

1929

Volltextzugriff (PDF)

ACUTE ENDOCARDITIS FOLLOWING GONORRHOEA

BMJ, 1913-07, Vol.2 (2741), p.68-68

Gill, A. Wilson

1913

Volltextzugriff (PDF)

Children's Civic Activities Necessary Factor in the New Civilization

The Annals of the American Academy of Political and Social Science, 1916-03, Vol.64 (1), p.197-203

Gill, Wilson L.

1916

Volltextzugriff (PDF)

A CASE OF MOLLUSCUM FIBROSUM

BMJ, 1915-10, Vol.2 (2858), p.533-534

Gill, A. Wilson

1915

Volltextzugriff (PDF)

A SECOND CASE OF Hb RENERT [β133(H11)Val → Ala]

Hemoglobin, 2001-01, Vol.25 (3), p.337-340

2001

Volltextzugriff (PDF)

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100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report

Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

Identification of novel regions of amplification and deletion within mantle cell lymphoma DNA by comparative genomic hybridization

Mutational analysis of class III receptor tyrosine kinases (C‐KIT, C‐FMS, FLT3) in idiopathic myelofibrosis

Identifying functionally important aberrations of Neurofibromin-1 (NF1) in non-small cell lung cancer (NSCLC)

Identifying functionally important aberrations of Neurofibromin-1 (NF1) in non-small cell lung cancer (NSCLC)

Guidelines for the measurement of BCR‐ABL1 transcripts in chronic myeloid leukaemia

Genetic testing in the assessment of living related kidney donors at risk of autosomal dominant polycystic kidney disease

Unraveling the role of C. difficile S-layer in infection and disease

Lineage‐specific chimerism monitoring after allogeneic haematopoietic stem cell transplantation: do we really know what we are measuring?

Predicting persistent inflammatory arthritis amongst early arthritis clinic patients in the UK: is musculoskeletal ultrasound required?

FLT3 internal tandem duplication mutations are rare in agnogenic myeloid metaplasia

c‐kit proto‐oncogene exon 8 in‐frame deletion plus insertion mutations in acute myeloid leukaemia

Long term lympho-haematopoietic reconstitution by umbilical cord blood stem cells following primary graft failure and autologous rescue

Long‐term dual donor derived haematopoietic reconstitution following double unrelated cord blood transplantation – single unit dominance is not always the case

Early indication of emergence from vegetative state derived from assessments with the SMART-a preliminary report

Guidelines for the measurement of BCRaABL1 transcripts in chronic myeloid leukaemia

Late Relapsing Childhood Lymphoblastic Leukemia

Late relapsing childhood lymphoblastic leukemia

BCR-ABL transcript with an e19a2 (c3a2) junction in classical chronic myeloid leukemia

HYSTERIA AND THE WORKMEN'S COMPENSATION ACT

ACUTE ENDOCARDITIS FOLLOWING GONORRHOEA

Children's Civic Activities Necessary Factor in the New Civilization

A CASE OF MOLLUSCUM FIBROSUM

A SECOND CASE OF Hb RENERT [β133(H11)Val → Ala]

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