PALAVRAS EM INGLÊS RELACIONADAS COM «MONOSOMY»
monosomy
examples
disorders
monosomy
form
aneuploidy
with
presence
only
chromosome
from
pair
partial
occurs
when
portion
copy
while
rest
copies
glossary
entry
genetics
home
reference
refers
segment
turner
syndrome
symptoms
diagnosis
healthline
also
called
gonadal
dysgenesis
bonnevie
ullrich
condition
found
females
trisomies
monosomies
boston
children
hospital
term
used
describe
absence
member
chromosomes
therefore
there
each
cell
body
familial
authors
hess
published
atlas
genet
cytogenet
oncol
haematol
medical
definitions
popular
10 LIVROS EM INGLÊS RELACIONADOS COM «MONOSOMY»
Descubra o uso de
monosomy na seguinte seleção bibliográfica. Livros relacionados com
monosomy e pequenos extratos deles para contextualizar o seu uso na literatura.
1
Monosomy: New Insights for the Healthcare Professional: 2011 ...
Therefore, in 24 adults with X monosomy and 19 healthy female controls, we
used SBM to compare (i) lobar CV, CT and SA; (ii) an index of hemispheric
gyrification; (iii) CT throughout the cortical sheet; and (iv) CT correlation between
cortical ...
2
Neoplastic Hematopathology
Monosomy 5/del(5q) may be seen in all FAB subtypes, but the frequency is
higher in AML- M6 (-60%) (50). Many of the patients with MDS or AML de novo
and abnormalities of chromosomes 5, 7, or both have had significant
occupational ...
3
Clinical Laboratory Medicine
Origins of aneuploidy. Nondisjunction (A), an important source of trisomy and
monosomy, occurs during mitosis or meiosis II when sister chromatids (or when
homologs in meiosis I, as shown in B) move together to the same daughter
nucleus.
Kenneth D. McClatchey, 2002
4
NORD Guide to Rare Disorders
Partial monosomy 8p with minimal dysmorphic signs. JMed Genet 1990;27:327-
329. Hutchinson R, et al. Distal 8p deletion (8p23.1-8pter): a common deletion?
JMed Genet 1992;29:407-41 1. Pecile V, et al. Deficiency of distal 8p-: report of ...
National Organization for Rare Disorders, 2003
5
The Principles of Clinical Cytogenetics
The only monosomies that have been reported are monosomy 21 and mosaic
monosomy 22. Monosomy 21 Mosaic monosomy 21 was reported in four
liveborns in the early literature [203—206]. The most prominent features included
...
Steven Gersen, Martha B. Keagle, 2013
6
Catalogue of Unbalanced Chromosome Aberrations in Man
Cooksley WEG, Firouz-Abadi A, Wallace DC: Monosomy of a "G" autosome in a
22 year-old female. Med J Aust 2: 178-180(1973). Dutrillaux B, Jonasson J,
Lauren K, Lejeune J, Lindsten J, Petersen GB, Saldana-Garcia P: An unbalanced
...
... Chromosome Abnormalities Monosomy 1q Ventricular septal defect
Monosomy 1q4 Ventricular septal defect, truncus arteriosus, pulmonary atresia,
pulmonary stenosis Monosomy 2q Atrial septal defect, coarctation, interrupted
aortic arch, ...
8
Catalog of Prenatally Diagnosed Conditions
The following convention has been adopted in listing chromosomal mosaicisms
in this catalog: (1) confined placental mosaicism with no apparent fetal
chromosomal aberration and, if known, biparental disomy is cited as trisomy (
monosomy) ...
9
A Dictionary of Genetic Damage
This dictionary is the first dictionary of genetic damage to be published. "A Dictionary of Genetic Damage" is provided for spelling reference, categorization reference, and information on the enormity of the genetic catastrophe.
Monosomy (when one chromosome lacks its homolog) in humans is very rare.
The majority of embryos with monosomies don't survive to be born. For liveborn
infants, the only autosomal monosomy reported in humans is monosomy 21.
Tara Rodden Robinson, 2011
10 NOTÍCIAS NAS QUAIS SE INCLUI O TERMO «MONOSOMY»
Conheça de que se fala nos meios de comunicação nacionais e internacionais e como se utiliza o termo
monosomy no contexto das seguintes notícias.
In Tufts Study, 10 Cancer Cases Found Among 125K Illumina NIPT …
This test in a now un-pregnant woman, showed both trisomy 13 and monosomy 18, according to the Bianchi team's report in JAMA. «GenomeWeb, jul 15»
Short stature and primary ovarian insufficiency possibly due to …
... immunofluorescence assays, may be the cause of a functional Xq partial monosomy leading to most Turner traits of the proband's phenotype. «7thSpace Interactive, jul 15»
Non-invasive Prenatal Testing (NIPT) Market Expected to Reach …
... miscarriage during the genetic screening test for common chromosomal abnormalities (trisomy 21, trisomy 18, trisomy 13, monosomy X, etc.). «CSO Australia, jun 15»
Non-invasive Prenatal Testing Market - Global Industry Analysis …
... Patau syndrome (trisomy 13), and Turner syndrome (monosomy X), and ... Edwards syndrome, Patau syndrome and monosomy X, and their ... «MarketWatch, jun 15»
Revolutionary prenatal screening check means parents-to-be can …
... and is more efficient at identifying chromosome conditions including Trisomy 21 (Down syndrome) and Monosomy X (Turner syndrome).”. «The Daily Telegraph, jun 15»
May News and Product Briefs
... including those associated with trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), trisomy 13 (Patau syndrome) and monosomy ... «Bio-IT World, jun 15»
First Confirmed Detection Of A Complete Molar Pregnancy With Cell …
... including trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), trisomy 13 (Patau syndrome), monosomy X (Turner syndrome) and ... «Laboratory Network, mai 15»
Barre boy receives a superhero homecoming
"Throughout this long series of test we found he had something called Monosomy 7," said Drew's mother Marie Bernier. Drew had a bone marrow transplant to ... «My Champlain Valley FOX44 & ABC22, mai 15»
Owen Shaner-McDermott, Be The Match Transplant Recipient
... multiple specialists, diagnosed him with MDS with monosomy 7. He needed a bone marrow transplant immediately to prevent the aggressive ... «KARE, mai 15»
Quest Diagnostics to Enhance Quality of Noninvasive Prenatal …
... including those associated with trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), trisomy 13 (Patau syndrome) and monosomy ... «SelectScience.net, mai 15»
