Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations [3]

Kristin Becker; Helen Hughes; Karol Howard; Maggie Armstrong; Devender Roberts; Edgar J. Lazda; John P. Short; Adam Shaw; Michael A. Patton; Marco Tartaglia

doi:10.1002/ajmg.a.31738

Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations [3]

Kristin Becker, Helen Hughes, Karol Howard, Maggie Armstrong, Devender Roberts, Edgar J. Lazda, John P. Short, Adam Shaw, Michael A. Patton, Marco Tartaglia

Ospedale Pediatrico Bambino Gesu

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

Original language	English
Pages (from-to)	1249-1252
Number of pages	4
Journal	American Journal of Medical Genetics, Part A
Volume	143
Issue number	11
DOIs	https://doi.org/10.1002/ajmg.a.31738
Publication status	Published - Jun 1 2007

ASJC Scopus subject areas

Genetics(clinical)

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10.1002/ajmg.a.31738

Cite this

@article{7e90342330104148a24514af5bba0433,

title = "Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations [3]",

author = "Kristin Becker and Helen Hughes and Karol Howard and Maggie Armstrong and Devender Roberts and Lazda, {Edgar J.} and Short, {John P.} and Adam Shaw and Patton, {Michael A.} and Marco Tartaglia",

year = "2007",

month = jun,

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doi = "10.1002/ajmg.a.31738",

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T1 - Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations [3]

AU - Becker, Kristin

AU - Hughes, Helen

AU - Howard, Karol

AU - Armstrong, Maggie

AU - Roberts, Devender

AU - Lazda, Edgar J.

AU - Short, John P.

AU - Shaw, Adam

AU - Patton, Michael A.

AU - Tartaglia, Marco

PY - 2007/6/1

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DO - 10.1002/ajmg.a.31738

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C2 - 17497712

AN - SCOPUS:34249907007

SN - 1552-4825

VL - 143

SP - 1249

EP - 1252

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 11

ER -

Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations [3]

ASJC Scopus subject areas

Access to Document

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