Uniparental disomy in cartilage-hair hypoplasia.

Sulisalo T, Mäkitie O, Sistonen P, Ridanpää M, el-Rifai W, Ruuskanen O, de la Chapelle A, Kaitila I
Eur J Hum Genet. 1997 5 (1): 35-42

PMID: 9156319

MeSH Terms (16)

Abnormalities, Multiple Child Child, Preschool Chromosome Mapping Chromosomes, Human, Pair 9 DNA Female Finland Genetic Markers Hair Humans Immunologic Deficiency Syndromes In Situ Hybridization, Fluorescence Osteochondrodysplasias Syndrome United States

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