Clinical implications of genetic defects in G proteins: The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy

Matthew D. Ringel; William F. Schwindinger; Michael A. Levine

doi:10.1097/00005792-199607000-00001

Clinical implications of genetic defects in G proteins: The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy

Matthew D. Ringel, William F. Schwindinger, Michael A. Levine

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

Original language	English (US)
Pages (from-to)	171-184
Number of pages	14
Journal	Medicine
Volume	75
Issue number	4
DOIs	https://doi.org/10.1097/00005792-199607000-00001
State	Published - Jul 1996

ASJC Scopus subject areas

Medicine(all)

Access to Document

10.1097/00005792-199607000-00001

Cite this

@article{f293822363634f6db10066836f9aa156,

title = "Clinical implications of genetic defects in G proteins: The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy",

author = "Ringel, {Matthew D.} and Schwindinger, {William F.} and Levine, {Michael A.}",

year = "1996",

month = jul,

doi = "10.1097/00005792-199607000-00001",

language = "English (US)",

volume = "75",

pages = "171--184",

journal = "Medicine",

issn = "0025-7974",

publisher = "Lippincott Williams and Wilkins",

number = "4",

}

TY - JOUR

T1 - Clinical implications of genetic defects in G proteins

T2 - The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy

AU - Ringel, Matthew D.

AU - Schwindinger, William F.

AU - Levine, Michael A.

PY - 1996/7

Y1 - 1996/7

UR - http://www.scopus.com/inward/record.url?scp=0029778906&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0029778906&partnerID=8YFLogxK

U2 - 10.1097/00005792-199607000-00001

DO - 10.1097/00005792-199607000-00001

M3 - Article

C2 - 8699958

AN - SCOPUS:0029778906

VL - 75

SP - 171

EP - 184

JO - Medicine

JF - Medicine

SN - 0025-7974

IS - 4

ER -

Clinical implications of genetic defects in G proteins: The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this