Related Experiment Videos

[Thin-layer chromatographic analysis of urinary homogentisic acid]

B Laars, H Lubs

Zeitschrift Fur Medizinische Laboratoriumsdiagnostik

|January 1, 1980

Abstract

No abstract available in PubMed .

Related Concept Videos

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

Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 gene.

Journal of medical genetics·2006

XLMR syndrome characterized by multiple respiratory infections, hypertelorism, severe CNS deterioration and early death localizes to distal Xq28.

American journal of medical genetics·1999

XLMR genes: update 1998.

American journal of medical genetics·1999

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

American journal of human genetics·1997

A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness.

Nature genetics·1996

X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12.

American journal of medical genetics·1996

See all related articles