(Q39846036)

15 September 2017

Genotype-phenotype correlations in MYCN-related Feingold syndrome (English)

1 reference

15 September 2017

Hans Scheffer

8

0 references

Han G. Brunner

10

object named as

Han G Brunner

1 reference

15 September 2017

9

Hans van Bokhoven

1 reference

15 September 2017

7

Dorien Lugtenberg

1 reference

15 September 2017

11

Arjan P M de Brouwer

1 reference

15 September 2017

Carlo L M Marcelis

1

1 reference

15 September 2017

Frans A Hol

2

1 reference

15 September 2017

Gail E Graham

3

1 reference

15 September 2017

Paul N M A Rieu

4

1 reference

15 September 2017

Richard Kellermayer

5

1 reference

15 September 2017

Rowdy P P Meijer

6

1 reference

15 September 2017

1 September 2008

1 reference

15 September 2017

1 reference

15 September 2017

29

1 reference

15 September 2017

1125-1132

1 reference

15 September 2017

9

1 reference

Expanding the clinical spectrum of MYCN-related Feingold syndrome

15 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Imperforate anus in Feingold syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Familial syndromic esophageal atresia maps to 2p23-p24.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Feingold syndrome: clinical review and genetic mapping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Identification of N-myc regulatory regions involved in embryonic expression.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Feingold syndrome--a cause of profound deafness.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

N-myc translation is initiated via an internal ribosome entry segment that displays enhanced activity in neuronal cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Vertebral defects in a patient with Feingold syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

A targeted mutation reveals a role for N-myc in branching morphogenesis in the embryonic mouse lung

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Predicting deleterious amino acid substitutions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Nmyc plays an essential role during lung development as a dosage-sensitive regulator of progenitor cell proliferation and differentiation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Activities of N-Myc in the developing limb link control of skeletal size with digit separation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

A new mathematical model for relative quantification in real-time RT-PCR

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Vertebral anomalies in a new family with ODED syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Growth deficiency in oculodigitoesophagoduodenal (Feingold) syndrome--case report and review of the literature.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Loss of N-myc function results in embryonic lethality and failure of the epithelial component of the embryo to develop

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

N-Myc and the cyclin-dependent kinase inhibitors p18Ink4c and p27Kip1 coordinately regulate cerebellar development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20750

7 January 2021

Identifiers

DOI

10.1002/HUMU.20750

1 reference

15 September 2017

1 reference