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Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer

Oncogene, 2002-10, Vol.21 (47), p.7277-7282

2002

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A homeobox gene, HLXB9 , is the major locus for dominantly inherited sacral agenesis

Nature genetics, 1998-12, Vol.20 (4), p.358-361

1998

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Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome

Human molecular genetics, 1995-06, Vol.4 (6), p.1027-1033

1995

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Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome

Human molecular genetics, 1993-10, Vol.2 (10), p.1577-1582

1993

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Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene

Genome research, 1998-08, Vol.8 (8), p.834

1998

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Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

Human molecular genetics, 1993-12, Vol.2 (12), p.2099-2107

1993

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Possible role for COMT in psychosis associated with velo-cardio-facial syndrome

The Lancet (British edition), 1992-11, Vol.340 (8831), p.1361-1362

1992

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Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11

American journal of human genetics, 1999-07, Vol.65 (1), p.247-249

1999

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Molecular Cytogenetic Characterization of the DiGeorge Syndrome Region Using Fluorescence in Situ Hybridization

Genomics (San Diego, Calif.), 1993-08, Vol.17 (2), p.403-407

1993

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Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11

Oncogene, 1990-06, Vol.5 (6), p.901-907

1990

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Preferential loss of maternal alleles in sporadic Wilms' tumour

Oncogene, 1990-11, Vol.5 (11), p.1665-1668

1990

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Structural rearrangements of the WT1 gene in Wilms' tumour cells

Oncogene, 1991-04, Vol.6 (4), p.595-599

1991

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Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein

Mammalian genome, 1997-05, Vol.8 (5), p.371-375

1997

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Loss of heterozygosity for chromosome region 11p15 in Wilms' tumours is not related to HRAS gene transforming mutations

Oncogene, 1991-07, Vol.6 (7), p.1147-1149

1991

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Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library

Human genetics, 1990-04, Vol.84 (5), p.417-423

1990

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The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11

Human genetics, 1989-05, Vol.82 (2), p.123-126

1989

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A Grounded Theory of Sport Injury-Related Growth

Sport, exercise, and performance psychology, 2017-02, Vol.6 (1), p.35-52

2017

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A systematic review of interventions to promote growth following adversity

Psychology of sport and exercise, 2020-05, Vol.48, p.101671, Article 101671

2020

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Sport Psychology Consultants’ Perspectives on Facilitating Sport-Injury-Related Growth

The Sport psychologist, 2019-09, Vol.33 (3), p.244-255

2019

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Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer

A homeobox gene, HLXB9 , is the major locus for dominantly inherited sacral agenesis

Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome

Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

Possible role for COMT in psychosis associated with velo-cardio-facial syndrome

Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11

Molecular Cytogenetic Characterization of the DiGeorge Syndrome Region Using Fluorescence in Situ Hybridization

Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11

Preferential loss of maternal alleles in sporadic Wilms' tumour

Structural rearrangements of the WT1 gene in Wilms' tumour cells

Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein

Loss of heterozygosity for chromosome region 11p15 in Wilms' tumours is not related to HRAS gene transforming mutations

Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library

The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11

A Grounded Theory of Sport Injury-Related Growth

A systematic review of interventions to promote growth following adversity

Sport Psychology Consultants’ Perspectives on Facilitating Sport-Injury-Related Growth

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