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Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.
Shrimpton, A E; Braddock, B R; Thomson, L L; Stein, C K; Hoo, J J.
Affiliation
  • Shrimpton AE; Department of Pediatrics, SUNY Upstate Medical University, Syracuse, NY, USA.
Clin Genet ; 66(6): 537-44, 2004 Dec.
Article in En | MEDLINE | ID: mdl-15521982
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Collection: 01-internacional Database: MEDLINE Main subject: Pseudopseudohypoparathyroidism / Chromosomes, Human, Pair 2 / Fibrous Dysplasia, Polyostotic / Intellectual Disability Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Clin Genet Year: 2004 Document type: Article Affiliation country: Estados Unidos Country of publication: Dinamarca
Search on Google
Add to My VHL
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Pseudopseudohypoparathyroidism / Chromosomes, Human, Pair 2 / Fibrous Dysplasia, Polyostotic / Intellectual Disability Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Clin Genet Year: 2004 Document type: Article Affiliation country: Estados Unidos Country of publication: Dinamarca