G. Sutherland

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The clinical significance of fragile sites on human chromosomes

E. Baker, G. Sutherland, 2000, Clinical genetics.

Heritable fragile sites on human chromosomes XII. Population Cytogenetics

G. Sutherland, 1985, Annals of human genetics.

Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers

R. Carter, G. Sutherland, A. J. Gardiner, 1976, Clinical genetics.

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

R. Cocciolone, D. Callen, G. Sutherland, 2001, Prenatal diagnosis.

A familial cryptic subtelomeric deletion 12p with variable phenotypic effect

L. Hinton, E. Baker, A. Dobbie, 2002, Clinical genetics.

A normal 46,XX infant with a 46,XX/ 69.XXY placenta: A major contribution to the placenta is from a resorbed twin

H. M. Chambers, D. Callen, G. Sutherland, 1991, Prenatal diagnosis.

Frequency of truly cryptic subtelomere abnormalities – a study of 534 patients and literature review

E. Haan, L. Hinton, S. Yu, 2005, Clinical genetics.

At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer

P. Devilee, A. Cleton-Jansen, C. Cornelisse, 1994, Genes, chromosomes & cancer.

AMP‐activated protein kinase isoenzyme family: subunit structure and chromosomal location

D. Power, B. Kemp, G. Sutherland, 1997, FEBS letters.

Diagnostic molecular genetics of the fragile X

J. Mulley, G. Sutherland, 1990, Clinical genetics.

Utilization of prenatal cytogenetic diagnosis in women of advanced maternal age in Australia, 1979–1982

J. Halliday, J. Pearn, N. Martin, 1985, Prenatal diagnosis.

Partial Seizures With Focal Epileptogenic Electroencephalographic Patterns in Three Related Female Patients With Fragile-X Syndrome

J. Manson, G. Sutherland, Rita Singh, 1999, Journal of child neurology.

Identification of the gene FMR2, associated with FRAXE mental retardation

J. Gécz, J. Mulley, A. Gedeon, 1996, Nature Genetics.

Myotonic dystrophy: from linkage with secretor status to mutation detection

G. Sutherland, 1993, Clinical genetics.

Three years' diagnostic experience with direct karyotyping of neonatal blood

G. Sutherland, I. Garnham, 1990, Clinical genetics.

Two unusual G‐band variants of the short arm of chromosome 9

H. Eyre, G. Sutherland, 1981, Clinical genetics.

Nxf and Fbxo33: novel seizure‐responsive genes in mice

A. Tsykin, R. W. Moyer, S. Koblar, 2004, The European journal of neuroscience.

DOWN'S SYNDROME IN SOUTH AUSTRALIA

G. Bloor, R. Carter, G. Sutherland, 1979, The Medical journal of Australia.

Fragile X syndrome and Fragile XE mental retardation

J. Mulley, G. Sutherland, 1996, Prenatal diagnosis.

A de novo mutation in sporadic nocturnal frontal lobe epilepsy

I. Scheffer, S. Berkovic, J. Mulley, 2000, Annals of Neurology.

At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer

P. Devilee, A. Cleton-Jansen, C. Cornelisse, 1994, Genes, chromosomes & cancer.

Prenatal diagnosis of the fragile X using thymidine induction

E. Baker, A. Hockey, S. Purvis-Smith, 1987, Prenatal diagnosis.

Predictive diagnosis for polycystic kidney disease using DNA markers

E. Haan, J. Mulley, A. Gedeon, 1990, The Medical journal of Australia.

Structural Organization and Chromosomal Localization of Three Human Galanin Receptor Genes

J. Shine, E. Baker, J. Dutton, 1998, Annals of the New York Academy of Sciences.

Observations on human amniotic fluid cell strains in serial culture

G. Sutherland, G. Sutherland, A. Bain, 1974, Journal of medical genetics.

Discordance between direct and PHA‐stimulated chromosome preparations from neonates

D. Callen, G. Sutherland, E. Haan, 1994, Clinical genetics.

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2

I. Scheffer, S. Berkovic, G. Sutherland, 1995, Nature Genetics.

Molecular genetics of human chromosome 16.

G. Sutherland, J. Mulley, D. Callen, 1987, Journal of medical genetics.

Identification, functional characterization, and chromosomal localization of USP15, a novel human ubiquitin-specific protease related to the UNP oncoprotein, and a systematic nomenclature for human ubiquitin-specific proteases.

G. Sutherland, X. W. Wang, R. Baker, 1999, Genomics.

Partial trisomy 3p syndrome

J. Reiss, L. Sheffield, G. Sutherland, 1986 .

Amniotic fluid macrophages and the antenatal diagnosis of anencephaly and spina bifida.

G. Sutherland, D. Brock, J. Scrimgeour, 1975, Journal of medical genetics.

Molecular characterization of murine and human OX40/OX40 ligand systems: identification of a human OX40 ligand as the HTLV‐1‐regulated protein gp34.

M. Seldin, G. Sutherland, F. Ramsdell, 1994, The EMBO journal.

Repeat offenders: Simple repeat sequences and complex genetic problems

R. Richards, G. Sutherland, 1996, Human mutation.

CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy.

I. Scheffer, D. Bertrand, S. Berkovic, 2001, American journal of human genetics.

Fragile sites-cytogenetic similarity with molecular diversity.

R. Richards, G. Sutherland, G. Sutherland, 1999, American journal of human genetics.

The molecular basis of fragile sites in human chromosomes.

R. Richards, G. Sutherland, G. Sutherland, 1995, Current opinion in genetics & development.

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

D. Loesch, G. Sutherland, J. Mulley, 1993, American journal of human genetics.

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

Andrew Menzies, Sarah Edkins, Sara Widaa, 2008, Nature Genetics.

LAIR-1, a novel inhibitory receptor expressed on human mononuclear leukocytes.

L Meyaard, L. Lanier, J. Phillips, 1997, Immunity.

Characterisation of a new rare fragile site easily confused with the fragile X.

G. Sutherland, E. Baker, G. Sutherland, 1992, Human molecular genetics.

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

G. Sutherland, D. Callen, A. Savoia, 2001, Genomics.

Dynamic mutation: possible mechanisms and significance in human disease.

R I Richards, R. Richards, G. Sutherland, 1997, Trends in biochemical sciences.

Simple tandem DNA repeats and human genetic disease.

R I Richards, R. Richards, G. Sutherland, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.

G. Sutherland, J. Mulley, G. Turner, 1989, American journal of medical genetics.

A refined physical map of the long arm of human chromosome 16.

C. E. Hildebrand, R. Stallings, R. Richards, 1991, Genomics.

A linkage map of microsatellite markers on the human X chromosome.

R. Richards, G. Sutherland, A. Donnelly, 1994, Genomics.

Dynamic mutation loci: allele distributions in different populations

K. Friend, S. Easteal, R. Richards, 1996, Annals of human genetics.

A Case of ring 20 chromosome with cardiac and renal anomalies

G. Sutherland, R. Burnell, LEON M. Stern, 1985, Australian paediatric journal.