(Q51831615)

English

Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies.

scientific article published on 28 October 2010

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14 January 2020

Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies (English)

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14 January 2020

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14 January 2020

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14 January 2020

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Issei Imoto

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14 January 2020

Yoshinori Aizu

3

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14 January 2020

Nobuhiko Okamoto

4

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14 January 2020

Seiji Mizuno

5

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14 January 2020

Kenji Kurosawa

6

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14 January 2020

Nana Okamoto

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14 January 2020

Shozo Honda

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14 January 2020

Satoshi Araki

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14 January 2020

Shuki Mizutani

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14 January 2020

Hironao Numabe

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14 January 2020

Tomoki Kosho

13

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14 January 2020

Yoshimitsu Fukushima

14

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14 January 2020

Hiroshi Mitsubuchi

15

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14 January 2020

Fumio Endo

16

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14 January 2020

Yasutsugu Chinen

17

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14 January 2020

Rika Kosaki

18

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14 January 2020

Torayuki Okuyama

19

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14 January 2020

Hirotaka Ohki

20

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14 January 2020

Hiroshi Yoshihashi

21

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14 January 2020

Masae Ono

22

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14 January 2020

Fumio Takada

23

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14 January 2020

Hiroaki Ono

24

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Mariko Yagi

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Hiroshi Matsumoto

26

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Yoshio Makita

27

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Akira Hata

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Johji Inazawa

29

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14 January 2020

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28 October 2010

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14 January 2020

Journal of Human Genetics

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110-124

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14 January 2020

https://scigraph.springernature.com/pub.10.1038/jhg.2010.129

0 references

Outcome of the routine assessment of patients with mental retardation in a genetics clinic

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

CONGENITAL ANOMALIES ASSOCIATED WITH IDIOPATHIC MENTAL RETARDATION.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Severe Mental Retardation in a Swedish County – II. Etiologic and Pathogenetic Aspects of Children Born 1959–1970

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

X chromosome array-CGH for the identification of novel X-linked mental retardation genes.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Chromosome 5q subtelomeric deletion syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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Molecular and clinical characterization of patients with overlapping 10p deletions

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Genomic microarrays in mental retardation: a practical workflow for diagnostic applications

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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14q12 Microdeletion syndrome and congenital variant of Rett syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Drayer's syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2-->qter).

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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1 reference

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1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

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Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

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1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Detection of subtelomere imbalance using MLPA: validation, development of an analysis protocol, and application in a diagnostic centre

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Diagnostic genome profiling in mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

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

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

Understanding variable expressivity in microdeletion syndromes.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

21 January 2018

The prevalence of mental retardation: a critical review of recent literature.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

7 January 2021

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Pure distal trisomy 2q: a rare chromosomal abnormality with recognizable phenotype

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

7 January 2021

based on heuristic

inferred from DOI database lookup

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

7 January 2021

based on heuristic

inferred from DOI database lookup

Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

7 January 2021

based on heuristic

inferred from DOI database lookup

High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical setting.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.129

7 January 2021

based on heuristic

inferred from DOI database lookup

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