A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?”

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	467-472
Number of pages	6
Journal	American Journal of Medical Genetics
Volume	95
Publication status	Published - 1 Jan 2000

Cite this

@article{3c255f83264d40c0957d855c94d693df,

title = "A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?”",

author = "NATACCI F. and Lucia CORRADO and PIERRI M. and ROSSETTI M. and ZUCCARINI C. and RIVA P. and M., \{MIOZZO AND L. LARIZZA\}",

year = "2000",

month = jan,

day = "1",

language = "English",

volume = "95",

pages = "467--472",

journal = "American Journal of Medical Genetics",

issn = "0148-7299",

publisher = "Wiley-Blackwell",

}

TY - JOUR

T1 - A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?”

AU - F., NATACCI

AU - CORRADO, Lucia

AU - M., PIERRI

AU - M., ROSSETTI

AU - C., ZUCCARINI

AU - P., RIVA

AU - M., MIOZZO AND L. LARIZZA

PY - 2000/1/1

Y1 - 2000/1/1

UR - https://iris.uniupo.it/handle/11579/10192

M3 - Article

SN - 0148-7299

VL - 95

SP - 467

EP - 472

JO - American Journal of Medical Genetics

JF - American Journal of Medical Genetics

ER -