No results for "Autosomal trisomies" (auto) in titles.

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1. Autosoma: Un autosoma o cromosoma somático es cualquier cromosoma que no sea sexual. En el humano, los cromosomas del par 1 al 22 son autosomas, y el par 23 corresponde a los cromosomas sexuales X e Y, también llamados heterocromosomas o ... [100%] 2023-05-26
2. Autosome: An autosome is any chromosome that is not a sex chromosome. The members of an autosome pair in a diploid cell have the same morphology, unlike those in allosomal (sex chromosome) pairs, which may have different structures. (Any chromosome other than a sex chromosome) [85%] 2023-12-24 [Chromosomes] [Cytogenetics]...
3. Autonoma: Autónomo hace referencia a varios artículos estos son algunos :. [85%] 2023-05-26
4. Autosome: Articles Most recent articles on Autosome Most cited articles on Autosome Review articles on Autosome Articles on Autosome in N Eng J Med, Lancet, BMJ Media Powerpoint slides on Autosome Images of Autosome Photos of Autosome Podcasts & MP3s on Autosome ... [85%] 2023-05-23 [Chromosomes]
5. Trisomie 9: Eine Trisomie 9, also eine Verdreifachung von Erbmaterial des 9. Chromosoms auf der Grundlage einer Genommutation, kommt vergleichsweise selten vor, meist in der Mosaik-Form oder als Partielle Trisomie 9 p (= Rethoré-Syndrom) in der Translokations-Form. [84%] 2023-07-21
6. Autosomal inheritance: Autosomal inheritance is inheritance of a genetic trait not on a sex chromosome. Autosomal recessive inheritance is the most common type of inheritance for retinal dystrophies. [80%] 2023-02-17 [Biology] [Genetics]...
7. Autosomal recessive: In genetics, a dominance relationship refers to how the alleles for a locus interact to produce a phenotype. There are three main kinds of dominance relationships: In general terms, a gene contributes to production or expression of some trait or ... [80%] 2023-03-21 [Physiology] [Genetic Disease]...
8. Autosomal recessive bestrophinopathy: Autosomal recessive bestrophinopathy is a rare genetic disorder characterized by central vision loss, retinopathy, absence of an electrooculogram light rise, and decreased electroretinogram. Other findings include dispersed punctate flecks, macular neurosensory retina fluid build-up, hyperopia, macular thinning, and (less ... (Medicine) [65%] 2023-08-16 [Genetic diseases and disorders]
9. Autosomal-dominante Makrothrombozytopenie: Die Autosomal-dominante Makrothrombozytopenie ist eine zur Gruppe der Makrothrombozytopenien gehörige angeborene Form der Thrombozytopenie mit Auftreten von Riesen-Thrombozyten. Synonyme sind: Glanzmann Thrombastenia, Autosomal Dominant; Thrombastenia Of Glanzmann And Naegeli, Autosomal Dominant; Bleeding disorder, platelet-type, 16, autosomal domin. [65%] 2023-05-11
10. Bases Autonomas: Bandera utilizada por Bases Autónomas en sus actos y publicaciones. fueron una organización neonazi que operó en España desde 1983 hasta mediados de los 90. Historia y acciones[editar] La organización fue fundada en Madrid en 1983,[1]​ bajo el nombre ... [62%] 2023-06-01
11. Accion Autonoma: Acción Autónoma , ''Avtonomnoe Deystvie'', (AD) es una [[federación]] [[revolución|revolucionaria]] y [[anarquista]] de [[Rusia]], [[Bielorrusia]] y [[Ucrania]], fundada en enero de [[2002]]. AD está compuesta de [[sindicalista]]s, [[Autonomía (filosofía y psicología)|autonomistas]], [[anarcocomunista]]s y ecologistas radicales. Acción Autónoma usa ... [60%] 2023-05-17
12. Scrobipalpa autonoma: Scrobipalpa autonoma is a moth in the family Gelechiidae. It was described by Povolný in 1969. (Species of moth) [60%] 2024-03-19 [Scrobipalpa] [Moths described in 1969]...
13. Autosomal recessive cerebellar ataxia: Autosomal recessive cerebellar ataxia (Orphanet 3711) describes a heterogeneous group of rare genetic disorders with an autosomal recessive inheritance pattern and a clinical phenotype involving cerebellar ataxia. [57%] 2022-10-17
14. Autosomal dominant cerebellar ataxia: Autosomal dominant cerebellar ataxia (ADCA) is a form of spinocerebellar ataxia inherited in an autosomal dominant manner. ADCA is a genetically inherited condition that causes deterioration of the nervous system leading to disorder and a decrease or loss of function ... [57%] 2023-09-23 [Autosomal dominant disorders] [Systemic atrophies primarily affecting the central nervous system]...
15. Autosomal dominant hypophosphatemic rickets: Autosomal dominant hypophosphatemic rickets (ADHR) is a rare hereditary disease in which excessive loss of phosphate in the urine leads to poorly formed bones (rickets), bone pain, and tooth abscesses. ADHR is caused by a mutation in the fibroblast growth ... [57%] 2023-11-14 [Endocrine diseases] [Skeletal disorders]...
16. Autosomal dominant hypophosphatemic rickets: Autosomal dominant hypophosphatemic rickets (ADHR) is a rare hereditary disease in which excessive loss of phosphate in the urine leads to poorly formed bones (rickets), bone pain, and tooth abscesses. ADHR is caused by a mutation in the fibroblast growth ... [57%] 2023-07-30 [Endocrine diseases] [Skeletal disorders]...
17. Autosomal recessive polycystic kidney disease: Autosomal recessive polycystic kidney disease (ARPKD) is the recessive form of polycystic kidney disease. It is associated with a group of congenital fibrocystic syndromes. (Medicine) [51%] 2023-11-06 [Kidney diseases] [Rare diseases]...
18. Autosomal recessive isolated ectopia lentis: Autosomal recessive isolated ectopia lentis is a rare hereditary disorder which is characterized by ectopia lentis (that is; a condition that displaces the position of the eye's lens) that is present in both eyes with no other significant abnormalities ... [51%] 2024-02-02 [Rare genetic syndromes]
19. Autosomal recessive multiple epiphyseal dysplasia: Autosomal recessive multiple epiphyseal dysplasia (ARMED), also called epiphyseal dysplasia, multiple, 4 (EDM4), multiple epiphyseal dysplasia with clubfoot or –with bilayered patellae, is an autosomal recessive congenital disorder affecting cartilage and bone development. The disorder has relatively mild signs and ... [51%] 2023-11-06 [Autosomal recessive disorders]
20. Autosomal dominant multiple pterygium syndrome: Multiple pterygium syndrome is a cutaneous condition inherited in an autosomal dominant fashion. Musician Patrick Henry Hughes has a type of this condition. (Medicine) [51%] 2023-11-17 [Genodermatoses] [Rare syndromes]...