Prader–Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study

Merlin G. Butler; Virginia Kimonis; Elisabeth Dykens; June A. Gold; Jennifer Miller; Roy Tamura; Daniel J. Driscoll

doi:10.1002/ajmg.a.38582

Prader–Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study

Merlin G. Butler
, Virginia Kimonis
, Elisabeth Dykens
, June A. Gold
, Jennifer Miller
, Roy Tamura
, Daniel J. Driscoll

Research output: Contribution to journal › Review article › peer-review

Original language	English
Pages (from-to)	368-375
Number of pages	8
Journal	American Journal of Medical Genetics, Part A
Volume	176
Issue number	2
DOIs	https://doi.org/10.1002/ajmg.a.38582
State	Published - Feb 2018
Externally published	Yes

ASJC Scopus Subject Areas

Genetics
Genetics(clinical)

Keywords

PWS genetic subtypes
Prader–Willi syndrome
genotype–phenotype correlations
longitudinal natural history study
mortality
rare disease consortium
Clinical Studies as Topic/history
History, 21st Century
United States
Humans
Mortality
National Institutes of Health (U.S.)
Obesity, Morbid/diagnosis
Rare Diseases/diagnosis
Age of Onset
Prader-Willi Syndrome/diagnosis
Outcome Assessment, Health Care

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10.1002/ajmg.a.38582

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@article{a857de3da5c44e0f9a4092df847fa7ab,

title = "Prader–Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study",

keywords = "PWS genetic subtypes, Prader–Willi syndrome, genotype–phenotype correlations, longitudinal natural history study, mortality, rare disease consortium, Clinical Studies as Topic/history, History, 21st Century, United States, Humans, Mortality, National Institutes of Health (U.S.), Obesity, Morbid/diagnosis, Rare Diseases/diagnosis, Age of Onset, Prader-Willi Syndrome/diagnosis, Outcome Assessment, Health Care",

author = "Butler, \{Merlin G.\} and Virginia Kimonis and Elisabeth Dykens and Gold, \{June A.\} and Jennifer Miller and Roy Tamura and Driscoll, \{Daniel J.\}",

note = "{\textcopyright} 2017 Wiley Periodicals, Inc.",

year = "2018",

month = feb,

doi = "10.1002/ajmg.a.38582",

language = "English",

volume = "176",

pages = "368--375",

journal = "American Journal of Medical Genetics, Part A",

issn = "1552-4825",

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T2 - A review of natural history study

AU - Butler, Merlin G.

AU - Kimonis, Virginia

AU - Dykens, Elisabeth

AU - Gold, June A.

AU - Miller, Jennifer

AU - Tamura, Roy

AU - Driscoll, Daniel J.

PY - 2018/2

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KW - Prader–Willi syndrome

KW - genotype–phenotype correlations

KW - longitudinal natural history study

KW - mortality

KW - rare disease consortium

KW - Clinical Studies as Topic/history

KW - History, 21st Century

KW - United States

KW - Humans

KW - Mortality

KW - National Institutes of Health (U.S.)

KW - Obesity, Morbid/diagnosis

KW - Rare Diseases/diagnosis

KW - Age of Onset

KW - Prader-Willi Syndrome/diagnosis

KW - Outcome Assessment, Health Care

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UR - https://www.mendeley.com/catalogue/473228e8-80d7-3b95-b613-f5071ffbc5a0/

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M3 - Review article

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VL - 176

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EP - 375

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 2

ER -

Prader–Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study

ASJC Scopus Subject Areas

Keywords

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