contiguous genes

См. также в других словарях:

• Contiguous gene syndrome — A disorder clearly involving multiple gene loci that are adjacent to one another. An example of a contiguous gene syndrome is Angelman syndrome. It is due to the loss of a series of genes from a region of chromosome 15 termed 15q13 15. (The… …   Medical dictionary

• Contiguous gene syndrome — A contiguous gene syndrome is a syndrome caused by abnormalities of 2 or more genes that are located next to each other on a chromosome. Prader Willi Syndrome, which is caused by the microdeletion of 15q11 13, is a common example. Prader Willi… …   Wikipedia

• Syndrome, contiguous gene — A disorder clearly involving multiple gene loci that are adjacent to one another. An example of a contiguous gene syndrome is Angelman syndrome. It is due to the loss of a series of genes from a region of chromosome 15 termed 15q13 15. (The… …   Medical dictionary

• Ocular albinism type 1 — Classification and external resources ICD 10 E70.3 OMIM 300500 DiseasesDB …   Wikipedia

• Intron — Introns, derived from the term intragenic regions and also called intervening sequence (IVS) [Cite web url = http://www.biochem.northwestern.edu/holmgren/Glossary/Definitions/Def I/intron.html title = intron (intervening sequence) author = Mark… …   Wikipedia

• EIF4H — Eukaryotic translation initiation factor 4H, also known as EIF4H, is a human gene.cite web | title = Entrez Gene: EIF4H eukaryotic translation initiation factor 4H| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

• List of genetic engineering topics — NOTOC # 3 end 5 end A Acentric chromosome Achondroplasia Active site Adam s Curse Adaptation Adenine Adenosine Adenosine diphosphate Adenovirus ADP Ala Alagille syndrome Albino Alcoholism Alkylating agent Allele Allele frequency Alleles… …   Wikipedia

• List of genetics-related topics — This is a list of terms related to genetics. NOTOC # * 3 end * 5 end A * Acentric chromosome * Achondroplasia * Active site * Adam s Curse * Adaptation * Adenine * Adenosine * Adenovirus * Adenosine diphosphate (ADP) * Ala * Alagille syndrome *… …   Wikipedia

• WBSCR22 — Williams Beuren syndrome chromosome region 22, also known as WBSCR22, is a human gene.cite web | title = Entrez Gene: WBSCR22 Williams Beuren syndrome chromosome region 22| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView …   Wikipedia

• WAGR syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 14025 ICD10 = ICD9 = ICDO = OMIM = 194072 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 2423 MeshID = D017624 WAGR syndrome is a rare genetic syndrome in which affected children are… …   Wikipedia

• LAT2 — Linker for activation of T cells family, member 2, also known as LAT2, is a human gene.cite web | title = Entrez Gene: LAT2 linker for activation of T cells family, member 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… …   Wikipedia