Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding
about
Further delineation of complex chromosomal rearrangements in fertile male using multicolor bandingA copy number variation map of the human genomeConsensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesNeonatal data on a cohort of 2889 infants born after ICSI (1991-1999) and of 2995 infants born after IVF (1983-1999).Neonatal outcome of 937 children born after transfer of cryopreserved embryos obtained by ICSI and IVF and comparison with outcome data of fresh ICSI and IVF cycles.Molecular cytogenetics and cytogenomics of brain diseases.A Novel de novo Balanced Reciprocal Translocation t(18;22) Associated with Recurrent Miscarriages: A Case Report.Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down Syndrome Cytogenetic Register and the Association of Clinical CytogeneticistsClinical outcomes of adjacent 1 segregation in a familial translocation t(8;18)(p21.3;p11.23).Schizophrenia susceptibility gene locus at Xp22.3.Discovery of common sequences absent in the human reference genome using pooled samples from next generation sequencing.A familial inverted duplication/deletion of 2p25.1-25.3 provides new clues on the genesis of inverted duplications.Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses.A chromosomal deletion map of human malformations.A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans.Characteristics of highly polymorphic segmental copy-number variations observed in Japanese by BAC-array-CGHSomatic genome variations in health and diseaseRapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities.Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGHAttitudes of Klinefelter men and their relatives towards TESE-ICSIComplex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder.Chromosome analysis: what and when to requestAnterior segment dysgenesis in mosaic Turner syndromeBalanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis.Prenatal screening of cytogenetic anomalies - a Western Indian experienceThe complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypesParental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies.Copy number variants, aneuploidies, and human diseaseConstitutional and acquired autosomal aneuploidyChromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in EuropeCytogenetics and gene discovery in psychiatric disorders.Genetic testing in children with autism spectrum disorders.Chromosomal Abnormalities in Infertile Men from Southern India.Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinationsMolecular cytogenetic characterization of two independent karyotypic anomalies in a patient with severe mental retardation and juvenile idiopathic arthritisBreakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohortCancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study.Benefits and drawbacks of preimplantation genetic diagnosis (PGD) for reciprocal translocations: lessons from a prospective cohort study.X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome
P2860
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P2860
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding
description
1992 nî lūn-bûn
@nan
1992 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Estimates of the frequency of ...... ing moderate levels of banding
@ast
Estimates of the frequency of ...... ing moderate levels of banding
@en
Estimates of the frequency of ...... ing moderate levels of banding
@en-gb
Estimates of the frequency of ...... ing moderate levels of banding
@nl
type
label
Estimates of the frequency of ...... ing moderate levels of banding
@ast
Estimates of the frequency of ...... ing moderate levels of banding
@en
Estimates of the frequency of ...... ing moderate levels of banding
@en-gb
Estimates of the frequency of ...... ing moderate levels of banding
@nl
prefLabel
Estimates of the frequency of ...... ing moderate levels of banding
@ast
Estimates of the frequency of ...... ing moderate levels of banding
@en
Estimates of the frequency of ...... ing moderate levels of banding
@en-gb
Estimates of the frequency of ...... ing moderate levels of banding
@nl
P2093
P2860
P356
P1476
Estimates of the frequency of ...... ing moderate levels of banding
@en
P2093
P2860
P356
10.1136/JMG.29.2.103
P407
P577
1992-02-01T00:00:00Z