Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene.

Clinical endocrinology - 1 Jul 2008

Iughetti Lorenzo, Sobrier Marie-Laure, Predieri Barbara, Netchine Irene, Carani Cesare, Bernasconi Sergio, Balli Fiorella, Amselem Serge

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Base Sequence
Share to DNA Mutational Analysis
Share to Dwarfism, Pituitary

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hormone Replacement Therapy

Share to Human Growth Hormone

Share to Infant

Share to Siblings

Source

Identifiers

PMID: 18088397
DOI: 10.1111/j.1365-2265.2007.03157.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene.PMID 18088397Read ↗

Mutations of the GH gene.Semantic proximity Read ↗

Isolated growth hormone deficiency due to the R183H mutation in GH1: Clinical analysis of a four-generation family.Semantic proximity Read ↗

Isolated GH deficiency with dominant inheritance: new mutations, new insights.Semantic proximity Read ↗

New GH-1 gene mutations: expanding the spectrum of causes of isolated growth hormone deficiency.Semantic proximity Read ↗

Genetics of isolated growth hormone deficiency.Semantic proximity Read ↗

Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiency.Semantic proximity Read ↗

Isolated growth hormone deficiency type IA due to a novel GH1 variant: a case report.Semantic proximity Read ↗

Genetic causes and treatment of isolated growth hormone deficiency-an update.Semantic proximity Read ↗

Growth hormone deficiency: an update.Semantic proximity Read ↗

Nonclassical GH Insensitivity: Characterization of Mild Abnormalities of GH ActionSemantic proximity Read ↗

Genetics of GH Deficiency: Insights From a Cohort of 203 PatientsSemantic proximity Read ↗

Genetic variations, clinical presentation and treatment outcome of isolated growth hormone deficiency type I and II: case series and review of the literatureSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.