Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region

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Metabolic Syndrome, Genetic Determinant, Genetics +9

Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.

L C Wilson, Kate E Leverton, M E Oude Luttikhuis et al. · PubMed · 1995 · 136 citations

Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals

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Expression of the heparan sulfate proteoglycan glypican-1 in the developing rodent

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Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype‐breakpoint correlations in 66 individuals

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