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

Clinical and molecular analysis of 30 patients with multiple lentigines LEOPARD syndrome.

Journal of medical genetics - 1 May 2004

Sarkozy A, Conti E, Digilio M Cristina, Marino B, Morini E, Pacileo G, Wilson M, Calabrò R, Pizzuti A, Dallapiccola B

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 Amino Acid Sequence
Share to Child, Preschool
Share to DNA Mutational Analysis
Share to Infant

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

Share to Intracellular Signaling Peptides and Proteins

Share to LEOPARD Syndrome

Share to Protein Tyrosine Phosphatase, Non-Receptor Type 11

Share to Protein Tyrosine Phosphatases

Source

Open in PubMed Open full text

Identifiers

PMID: 15121796
DOI: 10.1136/jmg.2003.013466
PMCID: PMC1735759

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and molecular analysis of 30 patients with multiple lentigines LEOPARD syndrome.PMID 15121796Read ↗

[LEOPARD syndrome].Semantic proximity Read ↗

The differential diagnosis of familial lentiginosis syndromesSemantic proximity Read ↗

[LEOPARD syndrome: A variant of Noonan syndrome with lentigines].Semantic proximity Read ↗

Leopard syndrome.Semantic proximity Read ↗

Genetic and phenotypic heterogeneity of multiple lentigines and precise diagnosis in four Chinese families with multiple lentigines.Semantic proximity Read ↗

Liddle syndrome in a Serbian family and literature review of underlying mutationsSemantic proximity Read ↗

[Leopard syndrome with clear phenotypic manifestations].Semantic proximity Read ↗

Leopard syndrome: a report of five cases from one family in two generations.Semantic proximity Read ↗

Molecular pathogenesis and management strategies of ectopia lentisSemantic proximity Read ↗

Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 GeneSemantic proximity Read ↗

LEOPARD Syndrome: Clinical Features and Gene MutationsSemantic proximity Read ↗

[Multiple lentigines (LEOPARD) syndrome. Case reports and review of the literature].Semantic proximity Read ↗

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