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Autosome
Bonnevie-Ullrich syndrome
Gonadal dysgenesis XO
Monosomia
Monosomies and deletions from the autosomes
Monosomy
Monosomy X
Turner syndrome
Turner's syndrome
Turner-Ullrich syndrome
XO syndrome

Traduction de «autosomal monosomy » (Anglais → Français) :

A partial autosomal monosomy with characteristics of a variable combination of developmental delay, intellectual disability, ectodermal, genitourinary and minor cardiac anomalies and specific dysmorphic features (prominent forehead and low-set ears).

monosomie non distale 12q


A rare partial autosomal monosomy with characteristics of weak fetal movements, severe infantile hypotonia and feeding difficulties that spontaneously improve with time, urogenital abnormalities (hypospadias or hypoplastic labia majora), global devel

syndrome de microdélétion 2p21 sans cystinurie


Monosomies and deletions from the autosomes

Monosomies et délétions des autosomes


A subgroup of therapy-related myeloid neoplasms (t-MN), associated with treatment of an unrelated neoplastic disease with radiation. The neoplastic cells typically harbor unbalanced aberrations of chromosomes 5 and 7 (monosomy 5/del(5q) and monosomy

leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux radiations




Bonnevie-Ullrich syndrome | gonadal dysgenesis XO | monosomy X | Turner syndrome | Turner's syndrome | Turner-Ullrich syndrome | XO syndrome

syndrome de Turner






Whole chromosome monosomy, meiotic nondisjunction

Monosomie d'un chromosome entier, non-disjonction méïotique


Whole chromosome monosomy, mosaicism (mitotic nondisjunction)

Monosomie d'un chromosome entier, mosaïque chromosomique (non-disjonction mitotique)




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'autosomal monosomy' ->

Date index: 2022-03-23
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