A familial deletion in the Prader-Willi syndrome region including the imprinting control region

Simone Schuffenhauer; Tina Buchholz; Sabine Stengel-Rutkowski; Karin Buiting; Heinrich Schmidt; Thomas Meitinger

doi:10.1002/(SICI)1098-1004(1996)8:3<288::AID-HUMU18>3.0.CO;2-Z

A familial deletion in the Prader-Willi syndrome region including the imprinting control region

Simone Schuffenhauer
, Tina Buchholz
, Sabine Stengel-Rutkowski
, Karin Buiting
, Heinrich Schmidt
, Thomas Meitinger

Ludwig-Maximilians-Universität München
Jugendmedizin der Universität
University Hospital of Essen

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

8 Scopus citations

Original language	English
Pages (from-to)	288-292
Number of pages	5
Journal	Human Mutation
Volume	8
Issue number	3
DOIs	https://doi.org/10.1002/(SICI)1098-1004(1996)8:3<288::AID-HUMU18>3.0.CO;2-Z
State	Published - 1996
Externally published	Yes

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10.1002/(SICI)1098-1004(1996)8:3<288::AID-HUMU18>3.0.CO;2-Z

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title = "A familial deletion in the Prader-Willi syndrome region including the imprinting control region",

author = "Simone Schuffenhauer and Tina Buchholz and Sabine Stengel-Rutkowski and Karin Buiting and Heinrich Schmidt and Thomas Meitinger",

year = "1996",

doi = "10.1002/(SICI)1098-1004(1996)8:3<288::AID-HUMU18>3.0.CO;2-Z",

language = "English",

volume = "8",

pages = "288--292",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "John Wiley and Sons Inc.",

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TY - JOUR

T1 - A familial deletion in the Prader-Willi syndrome region including the imprinting control region

AU - Schuffenhauer, Simone

AU - Buchholz, Tina

AU - Stengel-Rutkowski, Sabine

AU - Buiting, Karin

AU - Schmidt, Heinrich

AU - Meitinger, Thomas

PY - 1996

Y1 - 1996

UR - https://www.scopus.com/pages/publications/0029816730

U2 - 10.1002/(SICI)1098-1004(1996)8:3<288::AID-HUMU18>3.0.CO;2-Z

DO - 10.1002/(SICI)1098-1004(1996)8:3<288::AID-HUMU18>3.0.CO;2-Z

M3 - Article

C2 - 8889594

AN - SCOPUS:0029816730

SN - 1059-7794

VL - 8

SP - 288

EP - 292

JO - Human Mutation

JF - Human Mutation

IS - 3

ER -

A familial deletion in the Prader-Willi syndrome region including the imprinting control region

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