Identification of mtDNA mutation in a pedigree with gestational diabetes, deafness, Wolff-Parkinson-White syndrome and placenta accreta
Identification of mtDNA mutation in a pedigree with gestational diabetes, deafness, Wolff-Parkinson-White syndrome and placenta accreta
114-116
Aggarwal, Pritti
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Gill-Randall, R
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Wheatley, T
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Buchalter, M B
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Metcalfe, J
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Alcolado, John
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1 January 2001
Aggarwal, Pritti
d13e6516-5b53-4789-b627-115fcebd0d2b
Gill-Randall, R
dd410b99-2f6b-4c43-b91f-1457e7562523
Wheatley, T
f1c723d0-ebf7-4a06-b2b9-fc3d8fc56c4d
Buchalter, M B
7d878064-b178-497c-ae05-f279ba5fe566
Metcalfe, J
6d9d600e-b73b-4de0-831d-09b16f03c21d
Alcolado, John
5e4efcea-c089-407a-b5a2-bd6d212221c5
Aggarwal, Pritti, Gill-Randall, R, Wheatley, T, Buchalter, M B, Metcalfe, J and Alcolado, John
(2001)
Identification of mtDNA mutation in a pedigree with gestational diabetes, deafness, Wolff-Parkinson-White syndrome and placenta accreta.
Human Heredity, 51 (1/2), .
(doi:10.1159/000022950).
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Published date: 1 January 2001
Identifiers
Local EPrints ID: 482330
URI: http://eprints.soton.ac.uk/id/eprint/482330
ISSN: 0001-5652
PURE UUID: 3b05f953-83f1-4412-a03e-36c3309dbabc
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Date deposited: 26 Sep 2023 17:07
Last modified: 17 Mar 2024 04:51
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Author:
R Gill-Randall
Author:
T Wheatley
Author:
M B Buchalter
Author:
J Metcalfe
Author:
John Alcolado
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