Examples of using X-linked in English and their translations into German
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The disease corresponds to the X-linked PRA type 3 in humans.
Inheritance can be autosomal dominant, recessive or x-linked.
Differential diagnosis includes X-linked ocular albinism(OA1; see this term) and CSNB2.
Variable forms of inheritanc are associated with this disease dominant, recessive, X-linked, mitochondrial.
One x-linked RP carrier female with a normal standard ERG had a subnormal RmP3 on bright-flash ERG.
And only you have dimples, which are adorable,but they're also an x-linked dominant genetic trait.
The syndrome is classified as a X-linked osteopetrosis and is caused by mutations in the IKBKG(NEMO) gene Xq28.
An X-chromosomally inherited disease also exists at the B cell level: X-linked or Bruton's agammaglobulinemia.
Objective: X-linked congenital retinoschisis(XRS) is a relatively frequent retinal dystrophy affecting young males.
Arginine vasopressin receptor 2 Mutations in the vasopressin receptor 2 gene are responsible for x-linked nephrogenic diabetes insipidus.
X-linked intellectual disability is a disorder that predominantly affects men and can have highly variable clinical manifestations.
Normal skin samples tend to have alpha-5 chains in them butthese are rarely found in the skin samples of males with X-linked A5.
Genetic counseling Transmission is X-linked recessive in case of IKBKG mutations and autosomal-dominant in case of NFKBIA mutations.
Functional analysis of retinoschisin- A contribution to elucidate the molecular pathogenesis of X-linked juvenile retinoschisis.
The X-linked severe combined immunodeficiency(X-SCID) causes serious defects in cellular and humoral immunity.
The first and most common, approximately 90% of cases, is inherited in an X-linked fashion and is called X-linked Alport Syndrome XL-AS.
X-linked recessive hypophosphatemic rickets X-linked recessive hypophosphatemic rickets is caused by mutation in the CLCN5 and maybe also OCRL gene.
It can also be the answer in cases of advances maternal age,recurrent pregnancy loss, X-linked diseases or implantation failure.
Objective: X-linked congenital retinoschisis(XRS) is a relatively frequent retinal dystrophy affecting young males. Ophthalmoscopic changes might be difficult to detect.
They are divided according to the early or late onset of the disease and according to the mode of inheritance autosomal dominant, recessive, X-linked.
To ensure an equal amount of X-linked gene products in both sexes, dosage compensation has emerged as a molecular balancing mechanism.
Here, we were able to contribute specifically to the area of the macular dystrophies by cloning disease genes forconditions such as Sorsby fundus dystrophy, X-linked juvenile retinoschisis or Best vitelliforme macular dystrophy.
X-linked hypophosphatemia: The X-chromosomal PHEX gene(phosphate-regulating neutral endopeptidase, X-linked) encodes a peptidase which inhibits FGF23.
The differential diagnosis may include other forms of CL(ARC1 and ARCL2, and X-linked CL) and related syndromes(gerodermia osteodysplastica, wrinkly skin syndrome and De Barsy syndrome), together with the Ehlers-Danlos syndromes, Cantu syndrome and Costello syndrome see these terms.
X-linked familial short stature is a pseudo-autosomal dominant disorder caused by haploinsufficiency of a mutation in the pseudo-autosomal region of the x chromosome.
The difference in the dosage of X-linked genes between XX females and XY males is compensated by a mechanism called dosage compensation where one of the X chromosomes is inactivated.
