A C597→A polymorphism in the Norrie disease gene is associated with advanced retinopathy of prematurity in premature Kuwaiti infants

Disease Gene ◽

De novo mutations in the 5' regulatory region of the Norrie disease gene in retinopathy of prematurity

Journal of Medical Genetics ◽

10.1136/jmg.38.12.e46 ◽

2001 ◽

Vol 38 (12) ◽

pp. 46e-46 ◽

Cited By ~ 20

Author(s):

S J. Talks

Keyword(s):

Disease Gene ◽

De Novo ◽

Regulatory Region ◽

De Novo Mutations ◽

A C597→A Polymorphism in the Norrie Disease Gene Is Associated with Advanced Retinopathy of Prematurity in Premature Kuwaiti Infants

Journal of Biomedical Science ◽

10.1159/000065008 ◽

2002 ◽

Vol 9 (4) ◽

pp. 365-370 ◽

Cited By ~ 1

Author(s):

M.Z. Haider ◽

L.V. Devarajan ◽

M. Al-Essa ◽

H. Kumar

Keyword(s):

Disease Gene ◽

Identification of Missense Mutations in the Norrie Disease Gene Associated With Advanced Retinopathy of Prematurity

Archives of Ophthalmology ◽

10.1001/archopht.1997.01100150653015 ◽

1997 ◽

Vol 115 (5) ◽

pp. 651 ◽

Cited By ~ 87

Author(s):

Barkur S. Shastry

Keyword(s):

Disease Gene ◽

Missense Mutations ◽

Retinopathy of prematurity: Mutations in the Norrie disease gene and the risk of progression to advanced stages

Pediatrics International ◽

10.1046/j.1442-200x.2001.01361.x ◽

2001 ◽

Vol 43 (2) ◽

pp. 120-123 ◽

Cited By ~ 10

Author(s):

Mohammad Z Haider ◽

Lakshminaran V Devarajan ◽

Mazen Al-Essa ◽

Braham S Srivastva ◽

Harsh Kumar ◽

...

Keyword(s):

Disease Gene ◽

Norrie Disease ◽

Risk Of Progression ◽

Advanced Stages

Screening Preterm Newborns with Retinopathy of Prematurity for Mutation in Norrie Disease Gene

Pediatric Research ◽

10.1203/00006450-199904020-00804 ◽

1999 ◽

Vol 45 (4, Part 2 of 2) ◽

pp. 135A-135A

Author(s):

Mazen M Al-Essa ◽

Mohamed Z Haider ◽

Leventhal V Deverajan ◽

Haresh Kumar ◽

Nabil M Rashwan ◽

...

Keyword(s):

Disease Gene ◽

Norrie Disease ◽

Preterm Newborns

Missense Mutations in Norrie Disease Gene Are Not Associated with Advanced Stages of Retinopathy of Prematurity in Kuwaiti Arabs

Neonatology ◽

10.1159/000014199 ◽

2000 ◽

Vol 77 (2) ◽

pp. 88-91 ◽

Cited By ~ 12

Author(s):

M.Z. Haider ◽

L.V. Devarajan ◽

M. Al-Essa ◽

B.S. Srivastva ◽

H. Kumar ◽

...

Keyword(s):

Disease Gene ◽

Missense Mutations ◽

Norrie Disease ◽

Advanced Stages

Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematurity

Journal of Human Genetics ◽

10.1007/s100380170085 ◽

2001 ◽

Vol 46 (4) ◽

pp. 178-181 ◽

Cited By ~ 43

Author(s):

M. Hiraoka ◽

D. M. Berinstein ◽

M. T. Trese ◽

B. S. Shastry

Keyword(s):

Disease Gene ◽

Dinucleotide Repeat ◽

Repeat Region ◽

Deletion Mutations ◽

Norrie Disease ◽

Insertion And Deletion

Correlation of Ophthalmic Examination with Carrier Status in Females Potentially Harboring a Severe Norrie Disease Gene Mutation

Ophthalmology ◽

10.1016/j.ophtha.2007.04.064 ◽

2008 ◽

Vol 115 (4) ◽

pp. 730-733 ◽

Cited By ~ 1

Author(s):

Arif O. Khan ◽

Mohammed A. Aldahmesh ◽

Brian Meyer

Keyword(s):

Gene Mutation ◽

Disease Gene ◽

Carrier Status ◽

Ophthalmic Examination ◽

The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3

Human Molecular Genetics ◽

10.1093/hmg/1.2.83 ◽

1992 ◽

Vol 1 (2) ◽

pp. 83-89 ◽

Cited By ~ 29

Author(s):

K.B. Sims ◽

R.V. Lebo ◽

G. Benson ◽

C. Shalish ◽

D. Schuback ◽

...

Keyword(s):

Disease Gene ◽

Norrie Disease ◽

Gene Maps

Novel mutation at the initiation codon in the Norrie disease gene in two Japanese families

Human Genetics ◽

10.1007/bf00225085 ◽

1995 ◽

Vol 95 (1) ◽

Cited By ~ 13

Author(s):

Yasushi Isashiki ◽

Norio Ohba ◽

Toyoko Yanagita ◽

Naoko Hokita ◽

Norihito Doi ◽

...

Keyword(s):

Disease Gene ◽

Novel Mutation ◽

Initiation Codon ◽