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Narrowing the candidate region of Albright hereditary osteodystrophy-like syndrome by deletion mapping in a patient with an unbalanced cryptic translocation t(2;6)(q37.3;q26)

✍ Scribed by Giardino, Daniela ;Finelli, Palma ;Gottardi, Giulietta ;De Canal, Gabriella ;Monica, Matteo Della ;Lonardo, Fortunato ;Scarano, Gioacchino ;Larizza, Lidia


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
238 KB
Volume
122A
Category
Article
ISSN
0148-7299

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