Related Experiment Videos

Another case of maternal uniparental disomy chromosome 14 syndrome

M P Splitt, J A Goodship

American Journal of Medical Genetics

|October 23, 1997

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Evc regulates a symmetrical response to Shh signaling in molar development.

Journal of dental research·2013

Bases adjacent to mononucleotide repeats show an increased single nucleotide polymorphism frequency in the human genome.

Bioinformatics (Oxford, England)·2011

Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.

Clinical and experimental immunology·2008

FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality.

American journal of human genetics·2008

The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulation.

Molecular immunology·2007

A newly recognized, likely autosomal recessive syndrome comprising agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis, and other features.

American journal of medical genetics. Part A·2006

See all related articles