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Structural Organization and Chromosomal Localization of Three Human Galanin Receptor Genes.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 863, n. 1, p. 56, doi. 10.1111/j.1749-6632.1998.tb10683.x
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- Publication type:
- Article
γ-Heregulin: a fusion gene of DOC-4 and neuregulin-1 derived from a chromosome translocation.
- Published in:
- Oncogene, 1999, v. 18, n. 50, p. 7110, doi. 10.1038/sj.onc.1203136
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- Publication type:
- Article
Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discs.
- Published in:
- Oncogene, 1998, v. 17, n. 26, p. 3479, doi. 10.1038/sj.onc.1202249
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- Publication type:
- Article
A novel epithelial-expressed ETS gene, ELF3: human and murine cDNA sequences, murine genomic organization, human mapping to 1q32.2 and expression in tissues and cancer.
- Published in:
- Oncogene, 1997, v. 15, n. 20, p. 2449, doi. 10.1038/sj.onc.1201427
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- Publication type:
- Article
The "new genetics" and clinical practice.
- Published in:
- Medical Journal of Australia, 2003, v. 178, n. 8, p. 406, doi. 10.5694/j.1326-5377.2003.tb05262.x
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- Publication type:
- Article
Just how long can we live?
- Published in:
- Medical Journal of Australia, 2000, v. 173, p. 594, doi. 10.5694/j.1326-5377.2000.tb139353.x
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- Publication type:
- Article
C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain.
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- Journal of Human Genetics, 1999, v. 44, n. 6, p. 383, doi. 10.1007/s100380050183
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- Publication type:
- Article
GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 13, p. 1315, doi. 10.1093/hmg/ddh146
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- Publication type:
- Article
Aberrant CBFA2T3B gene promoter methylation in breast tumors.
- Published in:
- Molecular Cancer, 2004, v. 3, p. 22, doi. 10.1186/1476-4598-3-22
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- Publication type:
- Article
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer.
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- Genes, Chromosomes & Cancer, 1994, v. 9, n. 2, p. 101, doi. 10.1002/gcc.2870090205
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- Article
A Case of ring 20 chromosome with cardiac and renal anomalies.
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- Journal of Paediatrics & Child Health, 1985, v. 21, n. 4, p. 285, doi. 10.1111/j.1440-1754.1985.tb00167.x
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- Publication type:
- Article
The Mapping of the Trichohyalin Gene: Co-Localization with Profilaggrin, Involucrin, and Loricrin Genes.
- Published in:
- Journal of Investigative Dermatology, 1992, v. 99, n. 5, p. 542, doi. 10.1111/1523-1747.ep12667301
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- Publication type:
- Article
Phorbol ester-induced transcription of an immediate-early response gene by human T cells is inhibited by co-treatment with calcium ionophore.
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- Journal of Cellular Biochemistry, 1994, v. 54, n. 2, p. 135, doi. 10.1002/jcb.240540202
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- Publication type:
- Article
Fragile X syndrome and Fragile XE mental retardation.
- Published in:
- Prenatal Diagnosis, 1996, v. 16, n. 13, p. 1199, doi. 10.1002/(SICI)1097-0223(199612)16:13<1199::AID-PD95>3.0.CO;2-T
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- Publication type:
- Article
Prenatal diagnosis of the fragile X using thymidine induction.
- Published in:
- 1987
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- Publication type:
- journal article
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.
- Published in:
- Nature Genetics, 2002, v. 30, n. 4, p. 441
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- Publication type:
- Article
Mutant GABA<sub>A</sub> receptor γ2-subunit in childhood absence epilepsy and febrile seizures.
- Published in:
- Nature Genetics, 2001, v. 28, n. 1, p. 49, doi. 10.1038/88259
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- Publication type:
- Article
Febrile seizures and generalized epilepsy associated with a mutation in the Na<sup>+</sup>-channel ß1 subunit gene SCN1B.
- Published in:
- Nature Genetics, 1998, v. 19, n. 4, p. 366, doi. 10.1038/1252
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- Publication type:
- Article
Fcα/µ receptor is a single gene-family member closely related to polymeric immunoglobulin receptor encoded on Chromosome 1.
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- Immunogenetics, 2001, v. 53, n. 8, p. 709, doi. 10.1007/s00251-001-0375-y
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- Publication type:
- Article
DOWN'S SYNDROME IN SOUTH AUSTRALIA.
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- Medical Journal of Australia, 1979, v. 2, n. 2, p. 58, doi. 10.5694/j.1326-5377.1979.tb112703.x
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- Publication type:
- Article
Fcα/μ receptor mediates endocytosis of IgM-coated microbes.
- Published in:
- Nature Immunology, 2000, v. 1, n. 5, p. 441, doi. 10.1038/80886
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- Publication type:
- Article
Repeat offenders: Simple repeat sequences and complex genetic problems.
- Published in:
- Human Mutation, 1996, v. 8, n. 1, p. 1, doi. 10.1002/(SICI)1098-1004(1996)8:1<1::AID-HUMU1>3.0.CO;2-G
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- Publication type:
- Article
Moslecular and biological characterization of human 4-1BB and its ligands.
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- European Journal of Immunology, 1994, v. 24, n. 9, p. 2219, doi. 10.1002/eji.1830240943
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- Publication type:
- Article
NxfandFbxo33: novel seizure-responsive genes in mice.
- Published in:
- European Journal of Neuroscience, 2004, v. 20, n. 7, p. 1819, doi. 10.1111/j.1460-9568.2004.03646.x
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- Publication type:
- Article
The history and development of the Human Genetics Society of Australasia.
- Published in:
- 2008
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- Publication type:
- journal article
Myotonic dystrophy: from linkage with secretor status to mutation detection.
- Published in:
- Clinical Genetics, 1993, v. 43, n. 6, p. 273, doi. 10.1111/j.1399-0004.1993.tb03818.x
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- Publication type:
- Article
The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 167, doi. 10.1111/j.1399-0004.1990.tb03498.x
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- Publication type:
- Article
Diagnostic molecular genetics of the fragile X.
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- Clinical Genetics, 1990, v. 37, n. 1, p. 2, doi. 10.1111/j.1399-0004.1990.tb03383.x
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- Publication type:
- Article
Forgotten fragile sites and related phenomena.
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- Cytogenetic & Genome Research, 2003, v. 100, n. 1-4, p. 89, doi. 10.1159/000072842
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- Publication type:
- Article
Rare fragile sites.
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- Cytogenetic & Genome Research, 2003, v. 100, n. 1-4, p. 77, doi. 10.1159/000072840
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- Publication type:
- Article
Gene structure, alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative Bim.
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- Mammalian Genome, 2001, v. 12, n. 2, p. 163, doi. 10.1007/s003350010242
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- Publication type:
- Article
Culture of Cells from the Urine of Newborn Children.
- Published in:
- Nature, 1972, v. 239, n. 5369, p. 231, doi. 10.1038/239231a0
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- Publication type:
- Article
The Batten disease gene product (CLN3p) is a Golgi integral membrane protein.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 3, p. 523, doi. 10.1093/hmg/8.3.523
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- Publication type:
- Article
FMR2 Expression in Families with Fraxe Mental Retardation.
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- Human Molecular Genetics, 1997, v. 6, n. 3, p. 435, doi. 10.1093/hmg/6.3.435
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- Publication type:
- Article
Characterisation of a new rare fragile site easily confused with the fragile X.
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- Human Molecular Genetics, 1992, v. 1, n. 2, p. 111
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- Publication type:
- Article
Guidelines for the diagnosis of fragile X.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 2, p. 95, doi. 10.1111/j.1399-0004.1986.tb01228.x
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- Publication type:
- Article
Letters to the Editors:Detection of fragile sites on human chromosomes.
- Published in:
- Clinical Genetics, 1985, v. 28, n. 1, p. 95, doi. 10.1111/j.1399-0004.1985.tb01227.x
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- Publication type:
- Article
Detection of the fragile X chromosome and other fragile sites.
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- Clinical Genetics, 1984, v. 26, n. 4, p. 301, doi. 10.1111/j.1399-0004.1984.tb01063.x
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- Publication type:
- Article
Two unusual G-band variants of the short arm of chromosome 9.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 5, p. 331, doi. 10.1111/j.1399-0004.1981.tb00719.x
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- Publication type:
- Article
Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 1, p. 54, doi. 10.1111/j.1399-0004.1976.tb00009.x
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- Publication type:
- Article
Chromosomal mosaicism in amniotic fluid cell cultures.
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- Clinical Genetics, 1975, v. 7, n. 5, p. 400, doi. 10.1111/j.1399-0004.1975.tb00348.x
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- Publication type:
- Article
The antenatal diagnosis of trisomy 18.
- Published in:
- Clinical Genetics, 1974, v. 5, n. 2, p. 110, doi. 10.1111/j.1399-0004.1974.tb01670.x
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- Publication type:
- Article
Partial Seizures With Focal Epileptogenic Electroencephalographic Patterns in Three Related Female Patients With Fragile-X Syndrome.
- Published in:
- Journal of Child Neurology, 1999, v. 14, n. 2, p. 108, doi. 10.1177/088307389901400208
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- Publication type:
- Article
Maternal serum biochemistry identifies pregnancies at risk of fetal anomaly.
- Published in:
- 1990
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- Publication type:
- letter
Predictive diagnosis for polycystic kidney disease using DNA markers.
- Published in:
- Medical Journal of Australia, 1990, v. 152, n. 6, p. 287, doi. 10.5694/j.1326-5377.1990.tb120947.x
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- Publication type:
- Article
Presymptomatic testing for myotonic dystrophy by means of the linked DNA marker APOC2.
- Published in:
- Medical Journal of Australia, 1988, v. 149, n. 86, p. 326, doi. 10.5694/j.1326-5377.1988.tb120637.x
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- Publication type:
- Article
Buccal smears are not a useful diagnostic test!
- Published in:
- Medical Journal of Australia, 1984, v. 140, n. 6, p. 383, doi. 10.5694/j.1326-5377.1984.tb104122.x
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- Publication type:
- Article