(Q27004138)

English

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011

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Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 (English)

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author name string

A. Novelli

1

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F. R. Grati

2

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L. Ballarati

3

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L. Bernardini

4

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D. Bizzoco

5

1 reference

L. Camurri

6

1 reference

R. Casalone

7

1 reference

L. Cardarelli

8

1 reference

P. Cavalli

9

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R. Ciccone

10

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M. Clementi

11

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L. Dalprà

12

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M. Gentile

13

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G. Gelli

14

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P. Grammatico

15

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M. Malacarne

16

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A. M. Nardone

17

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V. Pecile

18

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G. Simoni

19

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O. Zuffardi

20

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D. Giardino

21

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language of work or name

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publication date

April 2012

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Ultrasound in Obstetrics and Gynecology

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39

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4

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384-8

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Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects

1 reference

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21 January 2018

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

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A copy number variation morbidity map of developmental delay

1 reference

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Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis

1 reference

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High-resolution array genomic hybridization in prenatal diagnosis

1 reference

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21 January 2018

Detecting genomic imbalances in prenatal diagnosis: main hurdles and recent advances

1 reference

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21 January 2018

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

1 reference

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21 January 2018

Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?

1 reference

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21 January 2018

Array technology in prenatal diagnosis.

1 reference

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21 January 2018

Emerging themes and new challenges in defining the role of structural variation in human disease

1 reference

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21 January 2018

Copy number variants, diseases and gene expression

1 reference

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21 January 2018

Structural variation in the human genome and its role in disease

1 reference

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21 January 2018

Controversies and challenges of array comparative genomic hybridization in prenatal genetic diagnosis

1 reference

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21 January 2018

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations

1 reference

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21 January 2018

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

1 reference

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21 January 2018

Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.

1 reference

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21 January 2018

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Complex and segmental uniparental disomy updated

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Cytogenetic contribution to uniparental disomy (UPD).

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Ethical issues raised by common copy number variants and single nucleotide polymorphisms of certain and uncertain significance in general medical practice

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Reciprocal translocations: a trap for cytogenetists?

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype

1 reference

https://api.crossref.org/works/10.1002%2FUOG.11092

21 January 2018

Identifiers

10.1002/UOG.11092

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