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

Borjeson-Forssman-Lehmann syndrome: a novel pituitary phenotype due to mutation in a novel gene.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Dec 2003

Dattani M T

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 Abnormalities, Multiple
Share to Bone Morphogenetic Proteins
Share to Fibroblast Growth Factor 8
Share to Fibroblast Growth Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, X-Linked

Share to Growth Hormone

Share to Hypopituitarism

Share to Pituitary Gland, Anterior

Source

Identifiers

PMID: 14714741
DOI: 10.1515/jpem.2003.16.9.1207

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Borjeson-Forssman-Lehmann syndrome: a novel pituitary phenotype due to mutation in a novel gene.PMID 14714741Read ↗

[Börjeson-Forssman-Lehmann syndrome].Semantic proximity Read ↗

The Börjeson–Forssman–Lehman syndrome (BFLS, MIM #301900)Semantic proximity Read ↗

Pituitary tumors in childhood: update of diagnosis, treatment and molecular genetics.Semantic proximity Read ↗

Molecular basis of pituitary dysfunction in mouse and human.Semantic proximity Read ↗

Variants in KAT6A and pituitary anomalies.Semantic proximity Read ↗

A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndrome.Semantic proximity Read ↗

Novel PHF6 mutation p.D333del causes Börjeson-Forssman-Lehmann syndrome.Semantic proximity Read ↗

Pituitary Pathology in Carney Complex PatientsSemantic proximity Read ↗

Genetic basis of endocrine disease: pituitary tumor pathogenesis.Semantic proximity Read ↗

HEREDITARY PITUITARY TUMOR SYNDROMES: GENETIC AND CLINICAL ASPECTS.Semantic proximity Read ↗

Novel mutations associated with combined pituitary hormone deficiency.Semantic proximity Read ↗

Familial Pituitary Tumor SyndromesSemantic proximity Read ↗

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