Related Experiment Videos

The mutational basis of the thalassemia syndromes

H H Kazazian, S Cho, J A Phillips

Progress in Medical Genetics

|January 1, 1977

Abstract

No abstract available in PubMed .

Related Concept Videos

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

Analysis of factor VIII gene inversion mutations in 166 unrelated haemophilia A families: frequency and utility in genetic counselling.

Haemophilia : the official journal of the World Federation of Hemophilia·2016

Molecular recognition of acute myeloid leukemia using aptamers.

Leukemia·2009

A new look at relationships between size at maturity and asymptotic size.

The American naturalist·2008

Isolated growth hormone deficiency type II caused by a point mutation that alters both splice site strength and splicing enhancer function.

Clinical genetics·2008

Mutations of the E1beta subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiency.

Molecular genetics and metabolism·2008

Cystic fibrosis gene variability in two southern Brazilian Amerindian populations: analysis of the deltaF508 mutation and the KM19 and XV2C haplotypes.

Human biology·2007

See all related articles