Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

D. Catchpoole; A. V. Smallwood; J. A. Joyce; A. Murrell; W. Lam; T. Tang; D. Munroe; W. Reik; P. N. Schofield; E. R. Maher

doi:10.1136/jmg.37.3.212

Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

D. Catchpoole, A. V. Smallwood, J. A. Joyce, A. Murrell, W. Lam, T. Tang, D. Munroe, W. Reik, P. N. Schofield, E. R. Maher

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

11 Citations (SciVal)

Original language	English
Pages (from-to)	212-215
Number of pages	4
Journal	Journal of Medical Genetics
Volume	37
Issue number	3
DOIs	https://doi.org/10.1136/jmg.37.3.212
Publication status	Published - 2000

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1136/jmg.37.3.212

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@article{69475d9d39424443842c71ab7594b794,

title = "Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome",

author = "D. Catchpoole and Smallwood, \{A. V.\} and Joyce, \{J. A.\} and A. Murrell and W. Lam and T. Tang and D. Munroe and W. Reik and Schofield, \{P. N.\} and Maher, \{E. R.\}",

year = "2000",

doi = "10.1136/jmg.37.3.212",

language = "English",

volume = "37",

pages = "212--215",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

number = "3",

}

TY - JOUR

T1 - Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

AU - Catchpoole, D.

AU - Smallwood, A. V.

AU - Joyce, J. A.

AU - Murrell, A.

AU - Lam, W.

AU - Tang, T.

AU - Munroe, D.

AU - Reik, W.

AU - Schofield, P. N.

AU - Maher, E. R.

PY - 2000

Y1 - 2000

UR - https://www.scopus.com/pages/publications/0034056510

U2 - 10.1136/jmg.37.3.212

DO - 10.1136/jmg.37.3.212

M3 - Letter

C2 - 10777363

AN - SCOPUS:0034056510

SN - 0022-2593

VL - 37

SP - 212

EP - 215

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

IS - 3

ER -

Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

ASJC Scopus subject areas

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