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List of works by Grant R Sutherland

A 5' flanking region of the metallothionein, MT2A, gene identifies two moderately frequent RFLPs.

scientific article

A linkage group with FRA16B (the fragile site at 16q22.1).

scientific article published in May 1989

A microsatellite marker within the duplicated D16S79 locus has a null allele; significance for linkage mapping

scientific article published on 01 January 1993

A new allele of alpha 1-antitrypsin: PI NADELAIDE.

scientific article published in January 1983

A new location for the human adenine phosphoribosyltransferase gene ( APRT ) distal to the haptoglobin ( HP ) and fra(16)(q23) ( FRAUD ) loci

article

A search for linkage in families with fragile sites

scientific article published on 01 January 1983

ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1.

scientific article

Aberrant CBFA2T3B gene promoter methylation in breast tumors

scientific article

Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1

article

An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15

article

Anticipation legitimized: unstable DNA to the rescue.

scientific article published in July 1992

Assignment of the human neuropeptide Y gene to chromosome 7p15.1 by nonisotopic in situ hybridization

scientific article published on 01 March 1995

Assignment of the human pyruvate carboxylase gene (PC) to 11q13.4 by fluorescence in situ hybridisation ⬇️

scientific article published on 01 January 1995

Assignment of the tyrosinase-related protein-2 gene (TYRP2) to human chromosome 13q31-q32 by fluorescence in situ hybridization: extended synteny with mouse chromosome 14

scientific article

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2 ⬇️

scientific article published on July 13, 1995

CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3.

scientific article

Characterization and chromosome location of the gene GSTZ1 encoding the human Zeta class glutathione transferase and maleylacetoacetate isomerase

scientific article

Characterization of the human Omega class glutathione transferase genes and associated polymorphisms

scientific article

Chromosomal Mapping of the Gene (PI9) Encoding the Intracellular Serpin Proteinase Inhibitor 9 to 6p25 by Fluorescencein SituHybridization

article

Chromosomal location of the human transketolase gene

scientific article (publication date: 1992)

Chromosomal location of the human tumor necrosis factor receptor genes ⬇️

scientific article published on January 1, 1991

Cloning, chromosomal mapping and characterization of the human metal-regulatory transcription factor MTF-1 ⬇️

scientific article

Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugs.

scientific article

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

scientific article (publication date: September 1999)

Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences

scientific article

Dinucleotide repeat polymorphisms at the D16S525, D16S359, D16S531 and D16S522 loci

scientific article published on 01 January 1994

Discordance between direct and PHA-stimulated chromosome preparations from neonates

scientific article published on 01 June 1994

Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation

scientific article

Distribution of alpha 1-antitrypsin (PI) phenotypes in chromosome abnormalities

scientific article published on 01 January 1981

Dynamic mutations on the move

scientific article

Experience with direct molecular diagnosis of fragile X ⬇️

scientific article published on June 1, 1992

Explanation for exclusive maternal origin for congenital form of myotonic dystrophy

scientific article published on 01 January 1993

Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16

article

Five dinucleotide repeat polymorphisms on human chromosome 16q24.2-q24.3.

scientific article published on 01 September 1993

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein

scientific article

Four dinucleotide repeat polymorphisms on human chromosome 16

scientific article published on 01 October 1993

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

scientific article

Fragile sites at 16q22 are not at the breakpoint of the chromosomal rearrangement in AMMoL

scientific article published on 01 April 1987

Fragile sites still breaking

scientific article published on 01 December 1998

Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome

scientific article

Further localization of ETS1 indicates that the chromosomal rearrangement in Ewing sarcoma does not occur at fra(11)(q23)

scientific article published on 01 February 1988

GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies

scientific article

Gene duplication of the human peptide YY gene (PYY) generated the pancreatic polypeptide gene (PPY) on chromosome 17q21.1

scientific article

Genetic length of a human chromosomal segment measured by recombination between two fragile sites

scientific article published on 01 July 1982

Genotype-phenotype relationships in fragile X syndrome: a family study.

scientific article

HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor

scientific article

Hereditary unstable DNA: a new explanation for some old genetic questions?

scientific article published in August 1991

Homozygotes for FRA16B are normal

scientific article published on 01 January 1999

Human and mouse homologues of the Drosophila melanogaster tweety (tty) gene: a novel gene family encoding predicted transmembrane proteins

scientific article

Human prostate-specific antigen (APS) is a member of the glandular kallikrein gene family at 19q13

scientific article

Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic loci

scientific article published on 01 January 1993

Interleukin 4 is at 5q31 and interleukin 6 is at 7p15

scientific article published on 01 August 1988

Is there a relationship between Wolfram syndrome carrier status and suicide?

scientific article (publication date: 8 April 2002)

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

scientific article published on 01 June 1992

Karyotypes found in the population declared at increased risk of Down syndrome following maternal serum screening

article

Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)

scientific article

Localization of a human receptor tyrosine kinase (ETK1) to chromosome region 3p11.2

scientific article

Localization of the adenosine A1 receptor subtype gene (ADORA1) to chromosome 1q32.1

scientific article

Localization of the adenosine A2b receptor subtype gene (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybrids

scientific article

Localization of the human GM-CSF receptor beta chain gene (CSF2RB) to chromosome 22q12.2-->q13.1

scientific article published on 01 January 1992

Localization of the human vitamin D 24-hydroxylase gene (CYP24) to chromosome 20q13.2-->q13.3

scientific article

Location and structure of the human FHR-5 gene

scientific article

Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site

scientific article published on 01 February 1991

Mapping of the human integrin beta 7 gene (ITG beta 7) to 12q13.13 by non-isotopic in situ hybridization

scientific article published in 1992

Mapping the human alpha globin gene complex to 16p13.2----pter

scientific article

Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein

scientific article

Molecular cloning and assignment of FAK2, a novel human focal adhesion kinase, to 8p11.2-p22 by nonisotopic in situ hybridization

scientific article published in March 1996

Molecular cloning and chromosomal mapping of the human homologue of MYB binding protein (P160) 1A (MYBBP1A) to 17p13.3

scientific article

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

scientific article (publication date: April 2002)

New classes of common fragile sites induced by 5-azacytidine and bromodeoxyuridine

scientific article published on 01 January 1985

No statistical association between common fragile sites and nonrandom chromosome breakpoints in cancer cells

scientific article published on 01 March 1988

Nxf and Fbxo33: novel seizure-responsive genes in mice

scientific article published in October 2004

Prenatal diagnosis of the fragile X using thymidine induction

scientific article published on 01 March 1987

Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1

scientific article published on 01 February 1990

Recombination and the fragile X.

scientific article published in June 1990

Recombination frequencies between Duchenne muscular dystrophy and intragenic markers in multigeneration families

scientific article published on 01 March 1988

Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16.

scientific article

Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes

scientific article

Sister chromatid exchange in aplastic anemia

scientific article published on 01 January 1981

Six dinucleotide repeat polymorphisms on human chromosome 16q12.1-q24.1.

scientific article published on 01 September 1993

Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies

scientific article published in February 2002

The "new genetics" and clinical practice

scientific article

The Batten disease gene product (CLN3p) is a Golgi integral membrane protein

scientific article

The gene for human carbonic anhydrase VI(CA6) is on the tip of the short arm of chromosome 1

scientific article (publication date: 1989)

The gene for human interleukin 7 (IL7) is at 8q12-13

scientific article

The gene for human leukemia inhibitory factor (LIF) maps to 22q12

scientific article (publication date: 1989)

The gene for the human IgA Fc receptor maps to 19q13.4

scientific article (publication date: April 1992)

The history and development of the Human Genetics Society of Australasia

scientific article published in August 2008

The human OTF1 locus which overlaps the CD3Z gene is located at 1q22-->q23

scientific article

The human metallothionein gene cluster is not disrupted in myelomonocytic leukemia

scientific article

The interleukin-4 receptor gene (IL4R) maps to 16p11.2–16p12.1 in human and to the distal region of mouse chromosome 7 ⬇️

scientific article published on 01 July 1991

The spectrum of SCN1A-related infantile epileptic encephalopathies

scientific article published in March 2007

Three dinucleotide repeat polymorphisms on human chromosome 16p13.11-p13.3.

scientific article published on 01 September 1993

Translocation breakpoint in t(11;14) in B-cell leukemia is not at the rare fragile site at 11q13.3

scientific article published on 01 March 1988

Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24

scientific article published on January 1, 1992

X-linked mental retardation with dystonic movements of the hands

scientific article

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

scientific article

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