Highly conserved non-coding sequences and the 18q critical region for short stature: a common mechanism of disease? (Q33316011)

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1 January 2020

title

Highly conserved non-coding sequences and the 18q critical region for short stature: a common mechanism of disease? (English)

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2

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Flavio Rizzolio

1

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1 January 2020

Orsetta Zuffardi

6

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1 January 2020

author name string

Cinzia Sala

3

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1 January 2020

Carla Tribioli

4

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1 January 2020

Roberto Ciccone

5

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1 January 2020

Natascia di Iorgi

7

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1 January 2020

Mohamad Maghnie

8

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1 January 2020

Daniela Toniolo

9

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language of work or name

English

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publication date

23 January 2008

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1 January 2020

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1 January 2020

volume

3

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issue

1

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1 January 2020

page(s)

e1460

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Creative Commons Attribution 4.0 International

1 January 2020

copyright license

start time

23 January 2008

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature.

21 June 2018

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Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?

21 June 2018

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21 June 2018

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Comparative genomic analysis reveals a distant liver enhancer upstream of the COUP-TFII gene

21 June 2018

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Highly conserved non-coding sequences are associated with vertebrate development

21 June 2018

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Arrays of ultraconserved non-coding regions span the loci of key developmental genes in vertebrate genomes

21 June 2018

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Long-range control of gene expression: emerging mechanisms and disruption in disease

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Patterns of seizures, hippocampal injury and neurogenesis in three models of status epilepticus in galanin receptor type 1 (GalR1) knockout mice

21 June 2018

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Ultraconserved Elements in the Human Genome

21 June 2018

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Transitions in histone acetylation reveal boundaries of three separately regulated neighboring loci

21 June 2018

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Neuralin-1 is a novel Chordin-related molecule expressed in the mouse neural plate

21 June 2018

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Multistep signaling and transcriptional requirements for pituitary organogenesis in vivo

21 June 2018

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SALL3, a new member of the human spalt-like gene family, maps to 18q23.

21 June 2018

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21 June 2018

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Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.

21 June 2018

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MRI of the hypophysis in a patient with the 18q- syndrome.

21 January 2018

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A new member of the spalt like zinc finger protein family, Msal-3, is expressed in the CNS and sites of epithelial/mesenchymal interaction.

21 January 2018

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Epigenetic control of the critical region for premature ovarian failure on autosomal genes translocated to the X chromosome: a hypothesis.

21 January 2018

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Genotype–phenotype mapping of chromosome 18q deletions by high-resolution array CGH: An update of the phenotypic map

21 January 2018

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A susceptibility gene for premature ovarian failure (POF) maps to proximal Xq28

21 January 2018

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12 December 2020

Hypogonadism in a patient with balanced X/18 translocation and pituitary hormone deficiency

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12 December 2020

Growth hormone insufficiency associated with haploinsufficiency at 18q23

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12 December 2020

The spectrum of growth abnormalities in children with 18q deletions

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12 December 2020

10.1371/JOURNAL.PONE.0001460

Identifiers

DOI

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