Alport syndrome and mental retardation: Clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR) [7]

I. Meloni; F. Vitelli; L. Pucci; R. B. Lowry; R. Tonlorenzi; E. Rossi; M. Ventura; G. Rizzoni; C. E. Kashtan; B. Pober; A. Renieri

Alport syndrome and mental retardation: Clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR) [7]

I. Meloni
, F. Vitelli
, L. Pucci
, R. B. Lowry
, R. Tonlorenzi
, E. Rossi
, M. Ventura
, G. Rizzoni
, C. E. Kashtan
, B. Pober
, A. Renieri

Pediatric Nephrology

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

Original language	English (US)
Pages (from-to)	359-365
Number of pages	7
Journal	Journal of medical genetics
Volume	39
Issue number	5
State	Published - 2002

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@article{67315c9acd2d4714a6937fc5aa9340b0,

title = "Alport syndrome and mental retardation: Clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR) [7]",

author = "I. Meloni and F. Vitelli and L. Pucci and Lowry, \{R. B.\} and R. Tonlorenzi and E. Rossi and M. Ventura and G. Rizzoni and Kashtan, \{C. E.\} and B. Pober and A. Renieri",

year = "2002",

language = "English (US)",

volume = "39",

pages = "359--365",

journal = "Journal of medical genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

number = "5",

}

TY - JOUR

T1 - Alport syndrome and mental retardation

T2 - Clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR) [7]

AU - Meloni, I.

AU - Vitelli, F.

AU - Pucci, L.

AU - Lowry, R. B.

AU - Tonlorenzi, R.

AU - Rossi, E.

AU - Ventura, M.

AU - Rizzoni, G.

AU - Kashtan, C. E.

AU - Pober, B.

AU - Renieri, A.

PY - 2002

Y1 - 2002

UR - https://www.scopus.com/pages/publications/18344377865

UR - https://www.scopus.com/pages/publications/18344377865#tab=citedBy

M3 - Letter

C2 - 12011158

AN - SCOPUS:18344377865

SN - 0022-2593

VL - 39

SP - 359

EP - 365

JO - Journal of medical genetics

JF - Journal of medical genetics

IS - 5

ER -

Alport syndrome and mental retardation: Clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR) [7]

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