Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374))

B. A. Bejjani; D. W. Stockton; R. A. Lewis; K. F. Tomey; D. K. Dueker; M. Jabak; W. F. Astle; J. R. Lupski

Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374))

B. A. Bejjani, D. W. Stockton, R. A. Lewis, K. F. Tomey, D. K. Dueker, M. Jabak, W. F. Astle, J. R. Lupski

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

2 Scopus citations

Original language	English
Pages (from-to)	1141
Number of pages	1
Journal	Human Molecular Genetics
Volume	9
Issue number	7
State	Published - Apr 12 2000

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Bejjani, B. A., Stockton, D. W., Lewis, R. A., Tomey, K. F., Dueker, D. K., Jabak, M., Astle, W. F., & Lupski, J. R. (2000). Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374)). Human Molecular Genetics, 9(7), 1141.

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title = "Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374))",

author = "Bejjani, {B. A.} and Stockton, {D. W.} and Lewis, {R. A.} and Tomey, {K. F.} and Dueker, {D. K.} and M. Jabak and Astle, {W. F.} and Lupski, {J. R.}",

year = "2000",

month = apr,

day = "12",

language = "English",

volume = "9",

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Bejjani, BA, Stockton, DW, Lewis, RA, Tomey, KF, Dueker, DK, Jabak, M, Astle, WF & Lupski, JR 2000, 'Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374))', Human Molecular Genetics, vol. 9, no. 7, pp. 1141.

Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374)). / Bejjani, B. A.; Stockton, D. W.; Lewis, R. A. et al.
In: Human Molecular Genetics, Vol. 9, No. 7, 12.04.2000, p. 1141.

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

TY - JOUR

T1 - Corrigendum

T2 - Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374))

AU - Bejjani, B. A.

AU - Stockton, D. W.

AU - Lewis, R. A.

AU - Tomey, K. F.

AU - Dueker, D. K.

AU - Jabak, M.

AU - Astle, W. F.

AU - Lupski, J. R.

PY - 2000/4/12

Y1 - 2000/4/12

UR - http://www.scopus.com/inward/record.url?scp=0034639934&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0034639934

SN - 0964-6906

VL - 9

SP - 1141

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 7

ER -

Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374))

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