BUKU BASA INGGRIS KAKAIT KARO «DISOMY»
Temukaké kagunané saka
disomy ing pilihan bibliografi iki. Buku kang kakait dening
disomy lan pethikan cekak kang padha kanggo nyediyakaké panggunané ing sastra Basa Inggris.
1
Genomic Imprinting and Uniparental
Disomy in Medicine: ...
This book will provide readers with the tools necessary to identify and treat diseases associated with nontraditional chromosomal inheritance.
Eric Engel, Stylianos E. Antonarakis, 2004
2
Uniparental
Disomy (UPD) in Clinical Genetics
Pan M, Li FT, Li Y, Jiang FM, Li DZ, Lau TK, Liao C (2013) Discordant results
between fetal karyotyping and non-invasive prenatal testing by maternal plasma
sequencing in a case of uniparental disomy 21 due to trisomic rescue. Prenat
Diagn ...
3
The Principles of Clinical Cytogenetics
In this thoroughly revised and expanded third edition of the highly praised classic, The Principles of Clinical Cytogenetics, Second Edition a panel of hands-on experts update their survey of the basic concepts and interpretations involved ...
Steven Gersen, Martha B. Keagle, 2013
4
Focus on Obesity Research
PWS individuals with the 15q11-q13 deletions exhibited significantly more self-
injury particularly skin picking than both the control group and the maternal
disomy subgroup (p < 0.01). The deletion subgroup displayed higher
compulsivity ...
5
Catalog of Prenatally Diagnosed Conditions
Uniparental disomy is the presence of two homologous chromosomes inherited
from the same parent: normally one of each of the homologous chromosomes
comes from each parent (biparental disomy). Theoretically, UPD will occur in a
third ...
6
Obesity Before Birth: Maternal and prenatal influences on ...
Thus, the fetus is delivered with PWS and normal cytogenetic findings, but with
maternal disomy 15. Maternal disomy 15 causing PWS is of two types:
heterodisomy and isodisomy. The disomic type may also impact on the
pregnancy and ...
7
Inherited Cardiac Disease
Table 7.1 The spectrum ofchromosome abnormalities with cardiovascular
malformations Cardiovascular malformation Chromosome abnormality Atrial
septal defect Paternal disomy 14; maternal disomy 16; microdeletion—1p36;
5q35; 6p25; ...
Perry Elliott, Pier D. Lambiase, Dhavendra Kumar, 2011
8
Mammalian Artificial Chromosomes: Methods and Protocols
distal-most portion (dis7), both maternal and paternal disomy give rise to
embryonic death. Detailed studies showed that the Matdi.dis7 embryos (and
placentas) were severely reduced in their growth, and they died at late fetal
stages (25).
V. Sgaramella, Sandro Eridani, 2004
The disomic line is usually normal, the exceptions, which involve uniparental
disomy and imprinting effects, are discussed in Chapter 2 1 . The most common
type of autosomal mosaicism involves chromosome 21. About 2-3% or more of ...
Orlando J. Miller, Eeva Therman, 2001
10
Catalogue of Unbalanced Chromosome Aberrations in Man
Stagni ML, della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G: Mosaic
trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and
uniparental disomy studies. Eur J Hum Genet 7: 421-426 ( 1999). Shaffer LG,
McCaskil!
BABAGAN WARTA KANG NGLEBOKAKÉ ARAN «DISOMY»
Weruhi yèn pawarta nasional lan internasional wis ngomongaké lan kepriyé aran
disomy digunakaké ing babagan warta iki.
Autism risk associated with parental age and with increasing …
Article | PubMed |; Ginsburg C, Fokstuen S, Schinzel A. The contribution of uniparental disomy to congenital development defects in children ... «Nature.com, Jun 15»
First Confirmed Detection of a Complete Molar Pregnancy with Cell …
In a complete molar pregnancy both sets of chromosomes are from the father a condition known as paternal uniparental disomy (UPD). «PharmiWeb.com, Mei 15»
(Epi)genotype–phenotype correlations in Beckwith–Wiedemann …
Altered expression at both gene clusters is observed in cases with mosaic paternal uniparental disomy (UPD) (20%: genome-wide UPD is ... «Nature.com, Apr 15»
Genetics and Genomics in Medicine
... Y-linked inheritance; heterogeneity and allele frequencies; gene regulation and epigenetics with uniparental disomy; genetic variation including chromosome ... «Nature.com, Apr 15»
UK's Deciphering Developmental Disorders Study Yields Diagnoses …
... diagnostic SNVs, indels, and CNVs, as well as six cases of uniparental disomy, where both copies of a chromosome came from one parent, ... «GenomeWeb, Des 14»
With Clinical Trials Underway, Agilent Anticipates 2014 FDA …
... use CGH arrays, despite the availability of newer chips that also have SNP content, which is useful in detecting loss of heterozygosity and uniparental disomy. «GenomeWeb, Nov 14»
Geneticists Seek Policies for Disclosing Incestuous Relationships …
... SNP-based arrays can identify regions of DNA with an absence of heterozygosity caused by uniparental disomy or identity by descent, and identification of ... «GenomeWeb, Nov 14»
Q&A: Baylor's Marilyn Li on the Clinical Application of Microarrays …
... but SNP arrays provide genotype information that allows the detection of uniparental disomy and copy number neutral loss of heterozygosity, ... «GenomeWeb, Nov 14»
With CombiMatrix Deal, Sequenom Becomes First Major NIPT …
... arrays, support a "much better analytical approach than quantitative CMA, because it allows the detection of triploidy and uniparental disomy. «GenomeWeb, Nov 14»
Agilent to Debut New CGH and SNP Arrays to Support Cyto, Cancer …
Until now, researchers who used Agilent's CGH arrays to detect uniparental disomy or copy-neutral loss of heterozygosity had to rely on SNP ... «GenomeWeb, Okt 14»
