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Search Results - Coleman-Campbell, Carrie M.
Search Results - Coleman-Campbell, Carrie M.
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Molecular characterization of histidinemia : identification of four missense mutations in the histidase gene
by
KAWAI, Yoko
,
MORIYAMA, Akihiko
,
ASAI, Kiyofumi
,
COLEMAN-CAMPBELL, Carrie M
,
SUMI, Satoshi
,
MORISHITA, Hideko
,
SUCHI, Mariko
Published in
Human genetics
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Molecular characterization of histidinemia: identification of four missense mutations in the histidase gene
by
Kawai, Yoko
,
Moriyama, Akihiko
,
Asai, Kiyofumi
,
Coleman-Campbell, Carrie M
,
Sumi, Satoshi
,
Morishita, Hideko
,
Suchi, Mariko
Published in
Human genetics
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An unusual N-terminal deletion of the laminin α3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
by
McLean, W. H. Irwin
,
Irvine, Alan D.
,
Hamill, Kevin J.
,
Whittock, Neil V.
,
Coleman-Campbell, Carrie M.
,
Mellerio, Jemima E.
,
Ashton, Gabrielle S.
,
Dopping-Hepenstal, Patricia J. H.
,
Eady, Robin A. J.
,
Jamil, Tanvir
,
Phillips, Rodney J.
,
Shabbir, S. Ghulam
,
Haroon, Tahir S.
,
Khurshid, Khawar
,
Moore, Jonathan E.
,
Page, Brian
,
Darling, Jonathan
,
Atherton, David J.
,
van Steensel, Maurice A. M.
,
Munro, Colin S.
,
Smith, Frances J. D.
,
McGrath, John A.
Published in
Human molecular genetics
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An unusual N-terminal deletion of the laminin 3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
by
McLean, W. H. I.
Published in
Human molecular genetics
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An unusual N-terminal deletion of the laminin ±3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
by
Irwin McLean, W H
,
Irvine, Alan D
,
Hamill, Kevin J
,
Whittock, Neil V
,
Coleman-Campbell, Carrie M
,
Mellerio, Jemima E
,
Ashton, Gabrielle S
,
Dopping-Hepenstal, Patricia J H
,
Eady, Robin A J
,
Jamil, Tanvir
,
Phillips, Roderic J
,
S. Ghulam Shabbir
Published in
Human molecular genetics
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An unusual N-terminal deletion of the laminin α3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
by
McLean, W. H. Irwin
,
Irvine, Alan D.
,
Hamill, Kevin J.
,
Whittock, Neil V.
,
Coleman-Campbell, Carrie M.
,
Mellerio, Jemima E.
,
Ashton, Gabrielle S.
,
Dopping-Hepenstal, Patricia J. H.
,
Eady, Robin A. J.
,
Jamil, Tanvir
,
Phillips, Roderic J.
,
Shabbir, S. Ghulam
,
Haroon, Tahir S.
,
Khurshid, Khawar
,
Moore, Jonathan E.
,
Page, Brian
,
Darling, Jonathan
,
Atherton, David J.
,
van Steensel, Maurice A. M.
,
Munro, Colin S.
,
Smith, Frances J. D.
,
McGrath, John A.
Published in
Human molecular genetics
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Article
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7
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An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
by
McLean, W H Irwin
,
Irvine, Alan D
,
Hamill, Kevin J
,
Whittock, Neil V
,
Coleman-Campbell, Carrie M
,
Mellerio, Jemima E
,
Ashton, Gabrielle S
,
Dopping-Hepenstal, Patricia J H
,
Eady, Robin A J
,
Jamil, Tanvir
,
Phillips, Roderic J
,
Shabbir, S Ghulam
,
Haroon, Tahir S
,
Khurshid, Khawar
,
Moore, Jonathan E
,
Page, Brian
,
Darling, Jonathan
,
Atherton, David J
,
Van Steensel, Maurice A M
,
Munro, Colin S
,
Smith, Frances J D
,
McGrath, John A
,
Phillips, Rodney J
Published in
Human molecular genetics
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Article
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8
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An unusual N-terminal deletion of the laminin a3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
by
MCLEAN, W. H
,
IRVINE, Alan D
,
PHILLIPS, Rodney J
,
GHULAM SHABBIR, S
,
HAROON, Tahir S
,
KHURSHID, Khawar
,
MOORE, Jonathan E
,
PAGE, Brian
,
DARLING, Jonathan
,
ATHERTON, David J
,
VAN STEENSEL, Maurice A. M
,
MUNRO, Colin S
,
HAMILL, Kevin J
,
SMITH, Frances J. D
,
MCGRATH, John A
,
WHITTOCK, Neil V
,
COLEMAN-CAMPBELL, Carrie M
,
MELLERIO, Jemima E
,
ASHTON, Gabrielle S
,
DOPPING-HEPENSTAL, Patricia J. H
,
EADY, Robin A. J
,
JAMIL, Tanvir
Published in
Human molecular genetics
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Article
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