
	Where results make sense

Topic: List of chromosomal translocations

Related Topics

Chromosomal translocation

Robertsonian translocation

Philadelphia chromosome

Centimorgan

Centromere

Patau syndrome

Cytogenetics

Infertility

Translocation

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	Trisomy 21: The Origin of Down Syndrome
		In meiosis, the pairs of chromosomes are supposed to split up and go to different spots in the dividing cell; this event is called "disjunction." However, occasionally one pair doesn't divide, and the whole pair goes to one spot.
		The 21st chromosome may actually hold 200 to 250 genes (being the smallest chromosome in the body in terms of total number of genes); but it's estimated that only a small percentage of those may eventually be involved in producing the features of Down syndrome.
		Because of the small size of the 21st chromosome and its association with Down syndrome, it is the second-most heavily mapped human chromosome.
	www.ds-health.com /trisomy.htm (1598 words)

	Cancer Genome Project
		In particular we are grateful to Felix Mitelman and his colleagues in providing information on more genes involved in uncommon translocations in leukaemias and lymphomas.
		Above is the working list of known cancer genes.
		The list has been annotated with information concerning chromosomal location, tumour types in which mutations are found, classes of mutation that contribute to oncogenesis and other genetic properties.
	www.sanger.ac.uk /genetics/CGP/Census (205 words)

	Molecular Cytogenetics Publications - Pat Heslop-Harrison & Trude
		Chromosomal variation in Crocus vernus Hill (Iridaceae) investigated by in situ hybridization of rDNA and a tandemly repeated sequence.
		Chromosome markers in the tetraploid wheat Aegilops ventricosa analysed by in situ hybridization.
		The absence of the somatic association of centromeres of homologous chromosomes in grass mitotic metaphases.
	www.le.ac.uk /biology/phh4/titles.htm (4278 words)

	Davis Human/Mouse Map : Useful internet addresses
		Chromosome 21 P1 & cDNA mapping and Syndb database
		Human chromosome 1 translocations, deletions and other abnormalities in neoplasms.
		University of Pennsylvania Human chromosome 22 Physical mapping data.
	www.ncbi.nlm.nih.gov /Omim/Homology/related.html (704 words)

	Genetic Disease Information
		A genetic disorder is a disease caused by abnormalities in an individual’s genetic material (genome).
		Because chromosomes are carriers of genetic material, such abnormalities in chromosome structure as missing or extra copies or gross breaks and rejoinings (translocations), can result in disease.
		For a list of all members in a particular city or state, enter the location without entering any names.
	www.ornl.gov /TechResources/Human_Genome/medicine/assist.html (2023 words)

	Primary Pulmonary Synovial Sarcoma: A Case Report and Review of Current Diagnostic and Therapeutic Standards -- ...
		IHC and chromosomal profile of synovial sarcoma compared with other primary lung neoplasms
		Cytogenetic studies of synovial sarcomas have revealed the chromosomal
		SYT gene from chromosome 18 to either of two homologous genes
	theoncologist.alphamedpress.org /cgi/content/full/9/3/339 (1253 words)

	links to resources on cytogenetics
		Mechanisms of Leukemogenesis: Chromosomal Translocations, Wendy Stock (Chair), Peter D. Educational Abstracts from the ASH.
		T-cell prolymphocytic leukemia: the Ataxia Telangiectasia gene -- a clonal proliferation of T-cells with a characteristic morphology, with a mature immunophenotype and often with karyotypic abnormalities on chromosome 14 (usually as an inversion between 14q11 and 14q32) and on chromosome 8 (usually as isochromosome 8q).
		Distribution of translocation-associated oncogenes in childhood ALL and Genes affected by chromosomal breakpoints in ALL.
	www.acor.org /ped-onc/diseases/translocations.html (497 words)

	Genetic Books
		This list was compiled prior to 1996, and is not updated regularly.
		You are made up of 23 chromosomes from your mother and 23 chromosomes from your father, and those 46 chromosomes contain a unique mixture of genes.
		Questions relating to exercise, physiotherapy, surgery, and the emotional effects of the disease are answered, and advice is given on the problems of schooling and choice of career.
	www.kumc.edu /gec/allbooks.html (7995 words)

	Publications
		Tease, C. Fisher, G. (1996): Cytogenetic and genetic studies of radiation-induced chromosome damage in mouse oocytes.
		I. Numerical and structural chromosome anomalies in metaphase II oocytes, pre- and post-implantation embryos
		Tease, C. (1996): Analysis using dual-colour fluorescence in situ hybridization of meiotic chromosome segregation in male mice heterozygous for a reciprocal translocation
	www.mgu.har.mrc.ac.uk /publications/index.html?date=1996 (1150 words)

	Treatments and prices for fertility treatment at The Bridge Centre
		For further information on other costs please ask for the detailed IUI price list.
		IVF+ICSI - because ICSI cannot exist without IVF, the term 'ICSI' is commonly used to encompass both the procedures of IVF and ICSI.
		In this document the procedures have been listed separately in order to explain the costings.
	www.thebridgecentre.co.uk /treatment1.htm (1301 words)

	Publikationen (Site not responding. Last check: 2007-10-14)
		Klicken Sie auf folgenden Link, um direkt zur Liste der Publikationen zu gelangen.
		By clicking on the following link, you can go directly to the list of publications.
		Before downloading, please make sure you have subscribed to the relevant journal.
	www.kip.uni-heidelberg.de /AG_Cremer/publications.html (53 words)

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