Pitfalls in homozygosity mapping

American Journal of Human Genetics

Volumn 67, Issue 5, 2000, Pages 1348-1351

  Miano, Maria G ^a,b   Jacobson, Samuel G ^c   Carothers, Andrew ^a   Hanson, Isabel ^a   Teague, Peter ^a   Lovell, Jill ^a   Cideciyan, Artur V ^c   Haider, Neena ^d,e   Stone, Edwin M ^e   Sheffield, Val C ^d,e   Wright, Alan F ^a  

^a WESTERN GENERAL HOSPITAL   (United Kingdom)

^b INSTITUTE OF GENETICS AND BIOPHYSICS ADRIANO BUZZATI TRAVERSO   (Italy)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

^d UNIVERSITY OF IOWA   (United States)

^e UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1; CONSANGUINITY; GENE MAPPING; GENETIC LINKAGE; HOMOZYGOSITY; PEDIGREE; PRIORITY JOURNAL;

EID: 0033765879     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9297(07)62966-8     Document Type: Article

References (4)

1. Long homozygous chromosomal segments in reference families from the Centre d’Etude du Polymorphisme Humain
2. A metric map of humans: 23,500 Loci in 850 bands
3. Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
4. Problems in dealing with linkage heterogeneity in autosomal recessive forms of retinitis pigmentosa