GeneralConnection.com ➔ Dictionary
Dictionary Search

monosomy

Synonyms

Noun

1. chromosomal aberration

2. chromosomal anomaly, chrosomal abnormality, chromosonal disorder

Usage
Partial 21q monosomy due to 21q inversion and 21 chromosome ring: two case reports. - European Society of Medicine
Congenital Anomalies in a Neonate With Partial Monosomy of Chromosome 21 q Arm: A Case Report - Cureus
The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development - Nature
Recommendations for management of positive monosomy X on cell-free DNA screening - Children's National
Monosomy X in Female Mice Influences the Regional Formation and Augments the Severity of Angiotensin II–Induced Aortopathies - American Heart Association Journals
Autosomal Monosomy in Man | NEJM - The New England Journal of Medicine
Overcoming the Odds of Familial Monosomy 7 - St. Jude Children's Research Hospital
Mutational landscape of AML patients with monosomy 7 - aml-hub.com
A rare finding of double Barr bodies and X-monosomy/X-trisomy mosaicism in a dog with presumed idiopathic epilepsy - Wiley Online Library
When a chromosome is lost: How do human cells react to monosomy? - Phys.org
Denise Richards Breaks Down While Explaining the Rare Disorder That Affects Her Daughter, Eloise - Bravo
Partial monosomy 18p and 21q due to a paternal reciprocal translocation leading to holoprosencephaly - Nature
Fluorescence in situ hybridization detection of chromosome 22 monosomy in pleural effusion cytology for the diagnosis of mesothelioma - Wiley & Sons
New-Onset Monosomy 7-Induced Pancytopenia in a 66-Year-Old Woman - Cureus
Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease - Nature
Monosomy 21 Seen in Live Born Is Unlikely to Represent True Monosomy 21: A Case Report and Review of the Literature - Wiley Online Library
DELE1 haploinsufficiency causes resistance to mitochondrial stress-induced apoptosis in monosomy 5/del(5q) AML - Nature
Hyperhaploid plasma cell myeloma characterized by poor outcome and monosomy 17 with frequently co-occurring TP53 mutations - Nature
Interpretation of cytogenetic results in multiple myeloma for clinical practice - Nature
Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study - Nature
Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21 - Nature
‘Non-classical’ HER2 FISH results in breast cancer: a multi-institutional study - Nature
SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations - Nature
High-level mosaic monosomy 21 in a 13-year-old girl: Case report and review of the literature - Wiley Online Library
Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome - Nature
BAP1 Loss on Immunocytochemistry and Its Association With Monosomy 3 in Uveal Melanoma Fine-Needle Aspirations - Wiley Online Library
Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukemia is an adverse prognostic factor: a report from the Children's Cancer Group - Nature
Monosomy 1p36: Report of a cohort of 13 Asian Indian patients - Wiley Online Library
Partial trisomy 3p/monosomy 9p with sex reversal - Witters - 2004 - obgyn.onlinelibrary.wiley.com
Therapy-related myelodysplastic syndrome with monosomy 7 and metastatic renal cell carcinoma successfully treated with nivolumab: two birds with one stone - Springer Nature Link
Refractory anaemia with ring sideroblasts and monosomy 7 in a 10-year-old child - Springer Nature Link
Genotype-outcome correlations in pediatric AML: the impact of a monosomal karyotype in trial AML-BFM 2004 - Nature
Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival - Haematologica
Towards mapping phenotypical traits in 18p− syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation - Nature
Deletions of chromosome 13 in multiple myeloma identified by interphase FISH usually denote large deletions of the q arm or monosomy - Nature
Transient juvenile myelomonocytic leukemia in the setting of PTPN11 mutation and Noonan syndrome with secondary development of monosomy 7 - Wiley Online Library
Successful Haploidentical Haematopoietic Stem Cell Transplant in a Rare Case of Bloom Syndrome Associated With Monosomy 7/MDS - Wiley Online Library
Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3)(q21;q26.2): a Bone Marrow Pathology Group study - Haematologica
Correction: Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development - PLOS
Fanconi Anemia patient with AML1 gene amplification and monosomy 7 in pre-transplant myelodysplasia (MDS) relapsing 7 years after successful allo-SCT - Nature
Birth of a Healthy Infant after Preimplantation Confirmation of Euploidy by Comparative Genomic Hybridization - The New England Journal of Medicine
Reproductive Medicine and Biology | Reproduction Journal - Wiley Online Library
Human blastocysts of normal and abnormal karyotypes display distinct transcriptome profiles - Nature
Monosomy 7 in Granulocytes and Monocytes in Myelodysplastic Syndrome - The New England Journal of Medicine
Pure monosomy and pure trisomy of 13q21.2–31.1 consequent to a familial insertional translocation: Exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1) - Wiley Online Library
Widespread DNA hypomethylation and differential gene expression in Turner syndrome - Nature
Karyotype complexity and prognosis in acute myeloid leukemia - Nature
Maternal age effect on the development of Prader–Willi syndrome resulting from upd(15)mat through meiosis 1 errors - Nature
Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT) - Nature
Myeloid malignancies with 5q and 7q deletions are associated with extreme genomic complexity, biallelic TP53 variants, and very poor prognosis - Nature
Severe Eosinophilia in Myelodysplastic Syndrome With a Defined and Rare Cytogenetic Abnormality - Frontiers
Multiple locations on chromosome 3 are the targets of specific deletions in uveal melanoma - Nature
Denise Richards Shares a Major Update on Teen Daughter, Eloise: "Such a Light" (EXCLUSIVE) - Bravo
Monosomy 20 as a pointer to dicentric (9;20) in acute lymphoblastic leukemia - Nature
Pediatric Bone Marrow Transplant for Bloom Syndrome: A Global First - OC Academy
Prognostic implications of abnormalities of chromosome 13 and the presence of multiple cytogenetic high-risk abnormalities in newly diagnosed multiple myeloma - Nature
Study Offers Updated Predictors of Uveal Melanoma - Review of Optometry
Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p - Nature
Texas A&M researchers studying reproductive abnormalities that cause sterility in horses - EurekAlert!
Progressive morphea of early childhood tracing Blaschko’s lines on the face: involvement of X chromosome monosomy in pathogenesis and clinical prognosis - Wiley Online Library
A Rare Combination of Chromosomal Abnormalities in an Infant With Turner Syndrome and Hypoplastic Left Heart Syndrome - Cureus
Genomic gains and losses influence expression levels of genes located within the affected regions: a study on acute myeloid leukemias with trisomy 8, 11, or 13, monosomy 7, or deletion 5q - Nature
Identify latent chromosomal aberrations relevant to myelodysplastic syndromes - Nature
The heterogeneous prognosis of patients with myelodysplastic syndrome and chromosome 5 abnormalities - Wiley & Sons
OBGYN - obgyn.onlinelibrary.wiley.com
Acute myeloid leukemia with monosomal karyotype at the far end of the unfavorable prognostic spectrum - Haematologica
Case report of de novo dup(18p)/del(18q) and r(18) mosaicism - Nature
Denise Richards opens up about parenting 'special-needs' daughter - USA Today
Kids aren’t little adults when it comes to pediatric MDS - St. Jude Children's Research Hospital
Foreign Language Equivalents
Foreign Language Equivalents of 'monosomy'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
monosoy,   monosommy,   monosoym,   monsomy,   omnosomy,   monosomyy,   mobosomy,   minosomy,   monoaomy,   mmonosomy,   monoosmy,   monosmy,   mnosomy,   monosoomy,   monosmoy,   momosomy,   mnoosomy,   monisomy,   moonsomy,   monoso,y,   monossomy,   monosony,   monosom,   monosomt,   monodomy,   monosimy,   monnosomy,   mpnosomy,   monsoomy,   monosomu,   ,onosomy,   moosomy,   onosomy,   monpsomy,   nonosomy,   moonosomy,   monoomy,   monoosomy,   monospmy
Words Starting with Letter - 'A'
a a battery a billion
a bit a bit much a capella singing
a cappella singing a couple of a few
a fortiori a good deal a great deal
a horizon a hundred a hundred and one
a hundred thousand a hundred times a kempis
a la carte a la mode a level
a little a lot a million
Go to Page 1              Go to Page 2 »   
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z