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

Risultato della ricerca: Contributo su rivista › Articolo in rivista › peer review

Lingua originale	Inglese
pagine (da-a)	467-472
Numero di pagine	6
Rivista	American Journal of Medical Genetics
Volume	95
Stato di pubblicazione	Pubblicato - 1 gen 2000

Altri file e collegamenti

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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-Liss Inc.",

}

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 -