Pseudoautosomal region — The pseudoautosomal regions, PAR1 and PAR3 are homologous sequences of nucleotides on the X and Y chromosomesThe pseudoautosomal regions get their name because any genes located within them (so far at least 29 have been found) [Blaschke RJ,… … Wikipedia
pseudoautosomal inheritance — inheritance of traits controlled by genes located in the pseudoautosomal regions of the sex chromosomes and mimicking the patterns of inheritance seen with autosomal genes … Medical dictionary
pseudoautosomal — adjective Describing genes in the X and Y chromosomes that behave like autosomes during meiosis … Wiktionary
Y chromosome — Human Y chromatid The Y chromosome is one of the two sex determining chromosomes in most mammals, including humans. In mammals, it contains the gene SRY, which triggers testis development if present. The human Y chromosome is composed of about 60 … Wikipedia
DHRSX — Dehydrogenase/reductase (SDR family) X linked Identifiers Symbols DHRSX; CXorf11; DHRS5X; DHRS5Y; DHRSXY; DHRSY; SDR46C1 External IDs … Wikipedia
Pseudoautosomale Region — Ausschnitt aus einer menschlichen Metaphase Spreitung. Eine Region in der pseudoautosomalen Region auf den kurzen Armen des X Chromosoms (links) und des Y Chromosoms (rechts oben) wurde mit Fluoreszenz in situ Hybridisierung nachgewiesen (grüne… … Deutsch Wikipedia
Pseudoautosomale Regionen — Ausschnitt aus einer menschlichen Metaphase Spreitung. Eine Region in der pseudoautosomalen Region auf den kurzen Armen des X Chromosoms (links) und des Y Chromosoms (rechts oben) wurde mit Fluoreszenz in situ Hybridisierung nachgewiesen (grüne… … Deutsch Wikipedia
XYY syndrome — Not to be confused with XXY (2 X s, Klinefelter s syndrome). XYY syndrome Classification and external resources Y chromosome ICD 10 Q … Wikipedia
X-inactivation — The Barr body is indicated by the arrow, it identifies the inactive X (Xi).] macroH2A1 staining. Arrow points to sex chromatin in DAPI stained cell nucleus, and to the corresponding sex chromatin site in the histone macroH2A1 staining.] X… … Wikipedia
Short stature homeobox gene — or SHOX is a gene on the X chromosome and Y chromosome which is associated with short stature in humans if mutated or present in only one copy (haploinsufficiency). PathologyThe gene was first found during a search for the cause of short stature… … Wikipedia
Acetylserotonin O-methyltransferase — Identifiers EC number 2.1.1.4 CAS number 9029 77 0 … Wikipedia
