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Items: 1 to 50 of 188

1.

Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort.

Kondkar AA, Sultan T, Almobarak FA, Kalantan H, Abu-Amero KK, Al-Obeidan SA.

BMC Res Notes. 2018 Oct 16;11(1):733. doi: 10.1186/s13104-018-3848-x.

2.

Analysis of CYP1B1 sequence alterations in patients with primary open-angle glaucoma of Saudi origin.

Abu-Amero KK, Sultan T, Al-Obeidan SA, Kondkar AA.

Clin Ophthalmol. 2018 Aug 10;12:1413-1416. doi: 10.2147/OPTH.S169943. eCollection 2018.

3.

Carriers of mitochondrial DNA macrohaplogroup L3 basal lineages migrated back to Africa from Asia around 70,000 years ago.

Cabrera VM, Marrero P, Abu-Amero KK, Larruga JM.

BMC Evol Biol. 2018 Jun 19;18(1):98. doi: 10.1186/s12862-018-1211-4.

4.

Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma.

Kondkar AA, Sultan T, Almobarak FA, Kalantan H, Al-Obeidan SA, Abu-Amero KK.

Clin Ophthalmol. 2018 Apr 12;12:701-706. doi: 10.2147/OPTH.S162999. eCollection 2018.

5.

Elevated levels of plasma tumor necrosis factor alpha in patients with pseudoexfoliation glaucoma.

Kondkar AA, Azad TA, Almobarak FA, Kalantan H, Al-Obeidan SA, Abu-Amero KK.

Clin Ophthalmol. 2018 Jan 17;12:153-159. doi: 10.2147/OPTH.S155168. eCollection 2018.

6.

Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort.

Kondkar AA, Azad TA, Almobarak FA, Kalantan H, Sultan T, Alsabaani NA, Al-Obeidan SA, Abu-Amero KK.

Genet Test Mol Biomarkers. 2018 Jan;22(1):74-78. doi: 10.1089/gtmb.2017.0159. Epub 2017 Nov 30.

PMID:
29190129
7.

Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort.

Kalantan H, Kondkar AA, Sultan T, Azad TA, Alsabaani NA, AlQahtani MA, Almummar A, Liu Y, Abu-Amero KK.

BMC Res Notes. 2017 Nov 29;10(1):652. doi: 10.1186/s13104-017-2996-8.

8.

A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles.

Abu-Amero KK, Kondkar AA, Khan AO.

BMC Res Notes. 2017 Nov 6;10(1):562. doi: 10.1186/s13104-017-2888-y.

9.

Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort.

Kondkar AA, Azad TA, Almobarak FA, Kalantan H, Sultan T, Al-Obeidan SA, Abu-Amero KK.

Genet Test Mol Biomarkers. 2017 Dec;21(12):754-758. doi: 10.1089/gtmb.2017.0147. Epub 2017 Oct 12.

PMID:
29022762
10.

Primary Congenital Glaucoma.

Abu-Amero KK, Edward DP.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2004 Sep 30 [updated 2017 Aug 17].

11.

Polymorphism rs547984 on human chromosome 1q43 is not associated with primary open angle glaucoma in a Saudi cohort.

Azad TA, Edward NB, Kondkar AA, Kalantan H, Altuwaijri S, Sultan T, Al-Mobarak FA, Al-Obeidan SA, Abu-Amero KK.

J Negat Results Biomed. 2017 Jun 26;16(1):12. doi: 10.1186/s12952-017-0077-0.

12.

Carriers of mitochondrial DNA macrohaplogroup R colonized Eurasia and Australasia from a southeast Asia core area.

Larruga JM, Marrero P, Abu-Amero KK, Golubenko MV, Cabrera VM.

BMC Evol Biol. 2017 May 23;17(1):115. doi: 10.1186/s12862-017-0964-5.

13.

Deep Capillary Macular Perfusion Indices Obtained with OCT Angiography Correlate with Degree of Nonproliferative Diabetic Retinopathy.

Sambhav K, Abu-Amero KK, Chalam KV.

Eur J Ophthalmol. 2017 Nov 8;27(6):716-729. doi: 10.5301/ejo.5000948.

PMID:
28362051
14.

NEW OBSERVATIONS REGARDING THE RETINOPATHY OF GENETICALLY CONFIRMED KEARNS-SAYRE SYNDROME.

Kozak I, Oystreck DT, Abu-Amero KK, Nowilaty SR, Alkhalidi H, Elkhamary SM, Mohamed S, Hamad MHA, Salih MA, Blakely EL, Taylor RW, Bosley TM.

Retin Cases Brief Rep. 2018 Fall;12(4):349-358. doi: 10.1097/ICB.0000000000000503.

PMID:
28296806
15.

Sirtuins Expression and Their Role in Retinal Diseases.

Balaiya S, Abu-Amero KK, Kondkar AA, Chalam KV.

Oxid Med Cell Longev. 2017;2017:3187594. doi: 10.1155/2017/3187594. Epub 2017 Jan 19. Review.

16.

Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients.

Kondkar AA, Edward NB, Kalantan H, Al-Kharashi AS, Altuwaijri S, Mohamed G, Sultan T, Azad TA, Abu-Amero KK.

J Negat Results Biomed. 2017 Feb 2;16(1):3. doi: 10.1186/s12952-017-0068-1.

17.

Carriers of human mitochondrial DNA macrohaplogroup M colonized India from southeastern Asia.

Marrero P, Abu-Amero KK, Larruga JM, Cabrera VM.

BMC Evol Biol. 2016 Nov 10;16(1):246.

18.

The genetics of nonsyndromic bilateral Duane retraction syndrome.

Abu-Amero KK, Khan AO, Oystreck DT, Kondkar AA, Bosley TM.

J AAPOS. 2016 Oct;20(5):396-400.e2. doi: 10.1016/j.jaapos.2016.06.008. Epub 2016 Sep 20.

PMID:
27658539
19.

Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma.

Abu-Amero KK, Kondkar AA, Mousa A, Almobarak FA, Alawad A, Altuwaijri S, Sultan T, Azad TA, Al-Obeidan SA.

Genet Test Mol Biomarkers. 2016 Oct;20(10):637-641. Epub 2016 Aug 19.

PMID:
27541204
20.

Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort.

Kondkar AA, Mousa A, Azad TA, Sultan T, Alawad A, Altuwaijri S, Al-Obeidan SA, Abu-Amero KK.

J Negat Results Biomed. 2016 Sep 29;15(1):17.

21.

Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma.

Kondkar AA, Mousa A, Azad TA, Sultan T, Almobarak FA, Alawad A, Altuwaijri S, Al-Obeidan SA, Abu-Amero KK.

Genet Test Mol Biomarkers. 2016 Nov;20(11):715-718. Epub 2016 Sep 12.

PMID:
27617586
22.

Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort.

Mousa A, Kondkar AA, Al-Obeidan SA, Azad TA, Sultan T, Osman EA, Abu-Amero KK.

Genet Test Mol Biomarkers. 2016 Sep;20(9):556-9. doi: 10.1089/gtmb.2016.0095. Epub 2016 Aug 15.

PMID:
27526043
23.

Analysis of toll-like receptor rs4986790 polymorphism in Saudi patients with primary open angle glaucoma.

Abu-Amero KK, Kondkar AA, Mousa A, Azad TA, Sultan T, Osman EA, Al-Obeidan SA.

Ophthalmic Genet. 2017 Mar-Apr;38(2):133-137. doi: 10.3109/13816810.2016.1151900. Epub 2016 Apr 11.

PMID:
27064537
24.

Resveratrol and Ophthalmic Diseases.

Abu-Amero KK, Kondkar AA, Chalam KV.

Nutrients. 2016 Apr 5;8(4):200. doi: 10.3390/nu8040200. Review.

25.

Duane Retraction Syndrome Associated with a Small X Chromosome Deletion.

Abu-Amero KK, Kondkar AA, Odan HA, Khan AO, Oystreck DT, Bosley TM.

Can J Neurol Sci. 2016 May;43(3):445-7. doi: 10.1017/cjn.2015.358. Epub 2016 Jan 25. No abstract available.

PMID:
26891113
26.

Analysis of Toll-Like Receptor 2 Polymorphism (rs5743704) in Saudi Patients with Primary Open-Angle Glaucoma.

Kondkar AA, Mousa A, Azad TA, Sultan T, Osman EA, Al-Obeidan SA, Abu-Amero KK.

Genet Test Mol Biomarkers. 2016 Apr;20(4):216-9. doi: 10.1089/gtmb.2015.0310. Epub 2016 Feb 11.

PMID:
26866668
27.

Duane retraction syndrome in a patient with Duchenne muscular dystrophy.

Bosley TM, Salih MA, Alkhalidi H, Oystreck DT, El Khashab HY, Kondkar AA, Abu-Amero KK.

Ophthalmic Genet. 2016 Sep;37(3):276-80. doi: 10.3109/13816810.2015.1039139. Epub 2016 Feb 5.

PMID:
26849454
28.

Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder.

Abu-Amero KK, Kondkar AA, Hellani AM, Bosley TM, Khan AO.

Neurosciences (Riyadh). 2016 Jan;21(1):72-4. doi: 10.17712/nsj.2016.1.20150098. No abstract available.

29.

Co-existence of m.10663T>C Mutation with Haplogroup L3f1b Background in a Patient with LHON.

Al-Kharashi M, Al-Kharashi A, Al-Obailan M, Kondkar AA, Abu-Amero KK.

Can J Neurol Sci. 2016 Mar;43(2):332-3. doi: 10.1017/cjn.2015.345. Epub 2016 Jan 11. No abstract available.

PMID:
26750644
30.

Assessment of the Knowledge and Attitudes of Saudi Mothers towards Newborn Screening.

Al-Sulaiman A, Kondkar AA, Saeedi MY, Saadallah A, Al-Odaib A, Abu-Amero KK.

Biomed Res Int. 2015;2015:718674. doi: 10.1155/2015/718674. Epub 2015 Oct 12.

31.

A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia.

Mohamed S, Hamad MH, Kondkar AA, Abu-Amero KK.

Saudi Med J. 2015 Oct;36(10):1229-32. doi: 10.15537/smj.2015.10.12127.

32.

Screening of the Seed Region of MIR184 in Keratoconus Patients from Saudi Arabia.

Abu-Amero KK, Helwa I, Al-Muammar A, Strickland S, Hauser MA, Allingham RR, Liu Y.

Biomed Res Int. 2015;2015:604508. doi: 10.1155/2015/604508. Epub 2015 Aug 24.

33.

Identification of 2 novel homozygous mutations in the methylmalonyl-CoA mutase gene in Saudi patients.

Mohamed S, Hamad MH, Abu-Amero KK.

Saudi Med J. 2015 Sep;36(9):1110-4. doi: 10.15537/smj.2015.9.12118.

34.

Neurometabolic Disorders-Related Early Childhood Epilepsy: A Single-Center Experience in Saudi Arabia.

Mohamed S, El Melegy EM, Talaat I, Hosny A, Abu-Amero KK.

Pediatr Neonatol. 2015 Dec;56(6):393-401. doi: 10.1016/j.pedneo.2015.02.004. Epub 2015 Apr 28.

35.

Carriers of Mitochondrial DNA Macrohaplogroup N Lineages Reached Australia around 50,000 Years Ago following a Northern Asian Route.

Fregel R, Cabrera V, Larruga JM, Abu-Amero KK, González AM.

PLoS One. 2015 Jun 8;10(6):e0129839. doi: 10.1371/journal.pone.0129839. eCollection 2015.

36.

Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population.

Abu-Amero KK, Helwa I, Al-Muammar A, Strickland S, Hauser MA, Allingham RR, Liu Y.

J Negat Results Biomed. 2015 Jun 4;14:10. doi: 10.1186/s12952-015-0029-5.

37.

Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Uebe S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zenteno JC, Nilgün Y, Zarnowski T, Pakravan M, Safieh LA, Jia L, Wang YX, Williams S, Paoli D, Schlottmann PG, Huang L, Sim KS, Foo JN, Nakano M, Ikeda Y, Kumar RS, Ueno M, Manabe S, Hayashi K, Kazama S, Ideta R, Mori Y, Miyata K, Sugiyama K, Higashide T, Chihara E, Inoue K, Ishiko S, Yoshida A, Yanagi M, Kiuchi Y, Aihara M, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Matsuda F, Yamashiro K, Gotoh N, Miyake M, Astakhov SY, Osman EA, Al-Obeidan SA, Owaidhah O, Al-Jasim L, Shahwan SA, Fogarty RA, Leo P, Yetkin Y, Oğuz Ç, Kanavi MR, Beni AN, Yazdani S, Akopov EL, Toh KY, Howell GR, Orr AC, Goh Y, Meah WY, Peh SQ, Kosior-Jarecka E, Lukasik U, Krumbiegel M, Vithana EN, Wong TY, Liu Y, Koch AE, Challa P, Rautenbach RM, Mackey DA, Hewitt AW, Mitchell P, Wang JJ, Ziskind A, Carmichael T, Ramakrishnan R, Narendran K, Venkatesh R, Vijayan S, Zhao P, Chen X, Guadarrama-Vallejo D, Cheng CY, Perera SA, Husain R, Ho SL, Welge-Luessen UC, Mardin C, Schloetzer-Schrehardt U, Hillmer AM, Herms S, Moebus S, Nöthen MM, Weisschuh N, Shetty R, Ghosh A, Teo YY, Brown MA, Lischinsky I; Blue Mountains Eye Study GWAS Team; Wellcome Trust Case Control Consortium 2, Crowston JG, Coote M, Zhao B, Sang J, Zhang N, You Q, Vysochinskaya V, Founti P, Chatzikyriakidou A, Lambropoulos A, Anastasopoulos E, Coleman AL, Wilson MR, Rhee DJ, Kang JH, May-Bolchakova I, Heegaard S, Mori K, Alward WL, Jonas JB, Xu L, Liebmann JM, Chowbay B, Schaeffeler E, Schwab M, Lerner F, Wang N, Yang Z, Frezzotti P, Kinoshita S, Fingert JH, Inatani M, Tashiro K, Reis A, Edward DP, Pasquale LR, Kubota T, Wiggs JL, Pasutto F, Topouzis F, Dubina M, Craig JE, Yoshimura N, Sundaresan P, John SW, Ritch R, Hauser MA, Khor CC.

Nat Genet. 2015 Jun;47(6):689. doi: 10.1038/ng0615-689c. No abstract available.

PMID:
26018902
38.

Association of total antioxidants level with glaucoma type and severity.

Mousa A, Kondkar AA, Al-Obeidan SA, Azad TA, Sultan T, Osman E, Abu-Amero KK.

Saudi Med J. 2015 Jun;36(6):671-7. doi: 10.15537/smj.2015.6.10697.

39.

A common variant near TGFBR3 is associated with primary open angle glaucoma.

Li Z, Allingham RR, Nakano M, Jia L, Chen Y, Ikeda Y, Mani B, Chen LJ, Kee C, Garway-Heath DF, Sripriya S, Fuse N, Abu-Amero KK, Huang C, Namburi P, Burdon K, Perera SA, Gharahkhani P, Lin Y, Ueno M, Ozaki M, Mizoguchi T, Krishnadas SR, Osman EA, Lee MC, Chan AS, Tajudin LS, Do T, Goncalves A, Reynier P, Zhang H, Bourne R, Goh D, Broadway D, Husain R, Negi AK, Su DH, Ho CL, Blanco AA, Leung CK, Wong TT, Yakub A, Liu Y, Nongpiur ME, Han JC, Hon DN, Shantha B, Zhao B, Sang J, Zhang N, Sato R, Yoshii K, Panda-Jonas S, Ashley Koch AE, Herndon LW, Moroi SE, Challa P, Foo JN, Bei JX, Zeng YX, Simmons CP, Bich Chau TN, Sharmila PF, Chew M, Lim B, Tam PO, Chua E, Ng XY, Yong VH, Chong YF, Meah WY, Vijayan S, Seongsoo S, Xu W, Teo YY, Cooke Bailey JN, Kang JH, Haines JL, Cheng CY, Saw SM, Tai ES; ICAARE-Glaucoma Consortium; NEIGHBORHOOD Consortium, Richards JE, Ritch R, Gaasterland DE, Pasquale LR, Liu J, Jonas JB, Milea D, George R, Al-Obeidan SA, Mori K, Macgregor S, Hewitt AW, Girkin CA, Zhang M, Sundaresan P, Vijaya L, Mackey DA, Wong TY, Craig JE, Sun X, Kinoshita S, Wiggs JL, Khor CC, Yang Z, Pang CP, Wang N, Hauser MA, Tashiro K, Aung T, Vithana EN.

Hum Mol Genet. 2015 Jul 1;24(13):3880-92. doi: 10.1093/hmg/ddv128. Epub 2015 Apr 10.

40.

Congenital cranial dysinnervation disorder in a boy with congenital mirror movements.

Al Shamrani M, Mahmoudi F, Abu-Amero KK, Khan AO.

J AAPOS. 2015 Apr;19(2):191-2. doi: 10.1016/j.jaapos.2014.10.028. Epub 2015 Mar 30.

PMID:
25838174
41.

MicroRNA profiling in intraocular medulloepitheliomas.

Edward DP, Alkatan H, Rafiq Q, Eberhart C, Al Mesfer S, Ghazi N, Al Safieh L, Kondkar AA, Abu Amero KK.

PLoS One. 2015 Mar 25;10(3):e0121706. doi: 10.1371/journal.pone.0121706. eCollection 2015.

42.

Utility of circulating microRNAs as clinical biomarkers for cardiovascular diseases.

Kondkar AA, Abu-Amero KK.

Biomed Res Int. 2015;2015:821823. doi: 10.1155/2015/821823. Epub 2015 Feb 1. Review.

43.

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Uebe S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zenteno JC, Nilgün Y, Zarnowski T, Pakravan M, Safieh LA, Jia L, Wang YX, Williams S, Paoli D, Schlottmann PG, Huang L, Sim KS, Foo JN, Nakano M, Ikeda Y, Kumar RS, Ueno M, Manabe S, Hayashi K, Kazama S, Ideta R, Mori Y, Miyata K, Sugiyama K, Higashide T, Chihara E, Inoue K, Ishiko S, Yoshida A, Yanagi M, Kiuchi Y, Aihara M, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Matsuda F, Yamashiro K, Gotoh N, Miyake M, Astakhov SY, Osman EA, Al-Obeidan SA, Owaidhah O, Al-Jasim L, Al Shahwan S, Fogarty RA, Leo P, Yetkin Y, Oğuz Ç, Kanavi MR, Beni AN, Yazdani S, Akopov EL, Toh KY, Howell GR, Orr AC, Goh Y, Meah WY, Peh SQ, Kosior-Jarecka E, Lukasik U, Krumbiegel M, Vithana EN, Wong TY, Liu Y, Koch AE, Challa P, Rautenbach RM, Mackey DA, Hewitt AW, Mitchell P, Wang JJ, Ziskind A, Carmichael T, Ramakrishnan R, Narendran K, Venkatesh R, Vijayan S, Zhao P, Chen X, Guadarrama-Vallejo D, Cheng CY, Perera SA, Husain R, Ho SL, Welge-Luessen UC, Mardin C, Schloetzer-Schrehardt U, Hillmer AM, Herms S, Moebus S, Nöthen MM, Weisschuh N, Shetty R, Ghosh A, Teo YY, Brown MA, Lischinsky I; Blue Mountains Eye Study GWAS Team; Wellcome Trust Case Control Consortium 2, Crowston JG, Coote M, Zhao B, Sang J, Zhang N, You Q, Vysochinskaya V, Founti P, Chatzikyriakidou A, Lambropoulos A, Anastasopoulos E, Coleman AL, Wilson MR, Rhee DJ, Kang JH, May-Bolchakova I, Heegaard S, Mori K, Alward WL, Jonas JB, Xu L, Liebmann JM, Chowbay B, Schaeffeler E, Schwab M, Lerner F, Wang N, Yang Z, Frezzotti P, Kinoshita S, Fingert JH, Inatani M, Tashiro K, Reis A, Edward DP, Pasquale LR, Kubota T, Wiggs JL, Pasutto F, Topouzis F, Dubina M, Craig JE, Yoshimura N, Sundaresan P, John SW, Ritch R, Hauser MA, Khor CC.

Nat Genet. 2015 Apr;47(4):387-92. doi: 10.1038/ng.3226. Epub 2015 Feb 23. Erratum in: Nat Genet. 2015 Jun;47(6):689.

44.

A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia. Molecular genetics report from Saudi Arabia.

Mohamed S, El-Kholy S, Al-Juryyan N, Al-Nemri AM, Abu-Amero KK.

Saudi Med J. 2015 Jan;36(1):113-6. doi: 10.15537/smj.2015.1.9697.

45.

Reply: To PMID 24969490.

Khan AO, Abu-Amero KK.

J AAPOS. 2014 Dec;18(6):622-3. doi: 10.1016/j.jaapos.2014.09.003. Epub 2014 Nov 13. No abstract available.

PMID:
25448154
46.

Genetics of keratoconus: where do we stand?

Abu-Amero KK, Al-Muammar AM, Kondkar AA.

J Ophthalmol. 2014;2014:641708. doi: 10.1155/2014/641708. Epub 2014 Aug 28. Review.

47.

Keratoconus is associated with increased copy number of mitochondrial DNA.

Abu-Amero KK, Kondkar AA, Azad TA, Sultan T, Kalantan H, Al-Muammar AM.

Mol Vis. 2014 Aug 27;20:1203-8. eCollection 2014.

48.

Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma.

Abu-Amero KK, Kondkar AA, Khan AO.

Ophthalmic Genet. 2016;37(1):98-101. doi: 10.3109/13816810.2014.924017. Epub 2014 Jun 9.

PMID:
24911043
49.

HOXA1 Mutations are Not Commonly Associated with Non-Syndromic Deafness.

Abu-Amero KK, Hagr Aa, Almomani MO, Azad TA, Alorainy IA, Oystreck DT, Bosley TM.

Can J Neurol Sci. 2014 Jul;41(4):448-51.

PMID:
24878468
50.

Microdeletions involving chromosomes 12 and 22 associated with syndromic Duane retraction syndrome.

Abu-Amero KK, Kondkar AA, Oystreck DT, Khan AO, Bosley TM.

Ophthalmic Genet. 2014 Sep;35(3):162-9. doi: 10.3109/13816810.2014.921317. Epub 2014 May 27.

PMID:
24865192

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