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

Variable clinical phenotypes of velocardiofacial syndrome in a pair of brothers.

Indian pediatrics - 1 Mar 2000

Ray M, Singhi P, Malhi P, Bhalla A

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 Child
Share to Cleft Palate
Share to Developmental Disabilities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Defects, Congenital

Share to Infant

Share to Syndrome

Source

Identifiers

PMID: 10750076

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Variable clinical phenotypes of velocardiofacial syndrome in a pair of brothers.PMID 10750076Read ↗

Velocardiofacial SyndromeSemantic proximity Read ↗

Velocardiofacial SyndromeSemantic proximity Read ↗

Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype.Semantic proximity Read ↗

Variable phenotypes in velocardiofacial syndrome with chromosomal deletion.Semantic proximity Read ↗

Clinical findings and phenotype in a toddler with 48,XXYY syndrome.Semantic proximity Read ↗

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromesSemantic proximity Read ↗

Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotype.Semantic proximity Read ↗

Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).Semantic proximity Read ↗

Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease.Semantic proximity Read ↗

Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.Semantic proximity Read ↗

Ehlers-Danlos syndrome: variable expression in sibs.Semantic proximity Read ↗

Facial phenotype at different ages and cardiovascular malformations in children with Williams-Beuren syndrome: a study from India.Semantic proximity Read ↗

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