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

Prenatal diagnosis of sporadic neurofibromatosis 1.

Lancet (London, England) - 11 Jan 1992

Lazaro C, Ravella A, Casals T, Volpini V, Estivill X

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 Base Sequence
Share to Chromosomes, Human, Pair 17
Share to Genetic Markers
Share to Neurofibromatosis 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymerase Chain Reaction

Share to Pregnancy

Share to Prenatal Diagnosis

Share to Recombination, Genetic

Source

Identifiers

PMID: 1345836
DOI: 10.1016/0140-6736(92)91024-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal diagnosis of sporadic neurofibromatosis 1.PMID 1345836Read ↗

Prenatal molecular diagnosis of L1-spectrum disorders.Semantic proximity Read ↗

Prenatal diagnosis of Charcot-Marie-Tooth disease.Semantic proximity Read ↗

Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs)Semantic proximity Read ↗

Prenatal molecular diagnosis of tuberous sclerosis complexSemantic proximity Read ↗

Prenatal diagnosis of Friedreich ataxia.Semantic proximity Read ↗

Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delaySemantic proximity Read ↗

Caution with noninvasive prenatal screening for single gene disorders: A case report of a COL1A1 variant in osteogenesis imperfecta.Semantic proximity Read ↗

Prenatal diagnosis for alpha1-antitrypsin deficiency.Semantic proximity Read ↗

Prenatal genetic confirmation of a COL4A1 mutation presenting with sonographic fetal intracranial hemorrhage.Semantic proximity Read ↗

Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation.Semantic proximity Read ↗

Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling.Semantic proximity Read ↗

Diagnosis of tuberous sclerosis in the prenatal period: a retrospective study of 240 cases and review of the literatureSemantic proximity Read ↗

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