Related Experiment Videos

Clinical and CSF studies in newborn infants with neurological abnormalities

S W De Souza, R D Milner

Archives of Disease in Childhood

|May 1, 1974

Abstract

No abstract available in PubMed .

Related Concept Videos

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

Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency.

The Journal of clinical endocrinology and metabolism·1998

Novel mutations and polymorphisms in the Fanconi anemia group C gene.

Human mutation·1996

Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families.

Journal of medical genetics·1994

Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein.

The Journal of clinical endocrinology and metabolism·1994

Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patient.

Acta paediatrica (Oslo, Norway : 1992). Supplement·1994

Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency.

The Journal of clinical endocrinology and metabolism·1993

See all related articles