(Q50772201)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22258158%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion (English)

1 reference

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20 January 2020

7

1 reference

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20 January 2020

Shin Hayashi

2

1 reference

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20 January 2020

author name string

Nana Okamoto

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22258158%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Ayako Masui

3

1 reference

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20 January 2020

Rika Kosaki

4

1 reference

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20 January 2020

Izumi Oguri

5

1 reference

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20 January 2020

Tomoko Hasegawa

6

1 reference

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20 January 2020

Yoshio Makita

8

1 reference

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20 January 2020

Akira Hata

9

1 reference

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20 January 2020

Keiji Moriyama

10

1 reference

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20 January 2020

Johji Inazawa

11

1 reference

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20 January 2020

publication date

19 January 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22258158%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

20 January 2020

published in

1 reference

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20 January 2020

volume

57

1 reference

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20 January 2020

issue

3

1 reference

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20 January 2020

page(s)

191-196

1 reference

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https://scigraph.springernature.com/pub.10.1038/jhg.2011.154

20 January 2020

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

Sex differences in the prevalence of human birth defects: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

Sex and congenital malformations: an international perspective.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

Effects of tongue volume reduction on craniofacial growth: A longitudinal study on orofacial skeletons and dental arches

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

Silencing of TGF-beta signalling by the pseudoreceptor BAMBI.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

The TGF-beta pseudoreceptor gene Bambi is dispensable for mouse embryonic development and postnatal survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

Identification of novel lung genes in bronchial epithelium by serial analysis of gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

The MAGUK protein MPP7 binds to the polarity protein hDlg1 and facilitates epithelial tight junction formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

Growth in head circumference from birth to fifteen years of age in Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

inferred from DOI database lookup

7 January 2021

based on heuristic

[Postero-anterior cephalometric features in Japanese children with malocclusion]

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.154

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/JHG.2011.154

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22258158%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference