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

Mild phenotypic expression of CHILD syndrome in two generations.

The British journal of dermatology - 1 Sept 2009

Alexandroff A B, Kinning E, Bamford M, Grzeschik K H, Milligan A, Camp R D R

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 Aged
Share to Body Height
Share to Ectodermal Dysplasia
Share to Exons

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

Share to Family

Share to Ichthyosiform Erythroderma, Congenital

Share to Syndrome

Source

Identifiers

PMID: 19614651
DOI: 10.1111/j.1365-2133.2009.09369.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 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

Mild phenotypic expression of CHILD syndrome in two generations.PMID 19614651Read ↗

On the use of the term "syndrome" in clinical genetics and birth defects epidemiology.Semantic proximity Read ↗

Mild phenotype of a large partial 13q trisomy.Semantic proximity Read ↗

Genetic causes of abnormal fetal development and inherited disease.Semantic proximity Read ↗

CHILD syndrome: clinical picture and diagnostic procedures.Semantic proximity Read ↗

Bibliography. Current world literature. Pediatric and heritable disorders.Semantic proximity Read ↗

Bibliography. Current world literature. Pediatric and heritable disorders.Semantic proximity Read ↗

Genetics, Syndromes, and Communication DisordersSemantic proximity Read ↗

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

Know Your Model: The role of sex in phenotype penetrance and severity.Semantic proximity Read ↗

Perspectives on craniofacial syndromes.Semantic proximity Read ↗

Sex differences in phenotypic manifestation and gene transmission in the Romano-Ward syndrome.Semantic proximity Read ↗

A pediatric genetic disorder diagnosed in adulthood.Semantic proximity Read ↗

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