Genotype-phenotype correlations in MYCN-related Feingold syndrome (Q39846036)

15 September 2017

title

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

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15 September 2017

Hans Scheffer

8

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Han G. Brunner

10

object named as

Han G Brunner

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15 September 2017

9

Hans van Bokhoven

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15 September 2017

7

Dorien Lugtenberg

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11

Arjan P M de Brouwer

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15 September 2017

Carlo L M Marcelis

1

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15 September 2017

Frans A Hol

2

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15 September 2017

Gail E Graham

3

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15 September 2017

Paul N M A Rieu

4

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15 September 2017

Richard Kellermayer

5

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15 September 2017

Rowdy P P Meijer

6

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15 September 2017

publication date

1 September 2008

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15 September 2017

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15 September 2017

volume

29

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15 September 2017

issue

9

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15 September 2017

page(s)

1125-1132

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Expanding the clinical spectrum of MYCN-related Feingold syndrome

15 September 2017

cites work

1 reference

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

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Vertebral defects in a patient with Feingold syndrome

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7 January 2021

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

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

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

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7 January 2021

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

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Identifiers

DOI

10.1002/HUMU.20750

1 reference

15 September 2017

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