35 related articles for article (PubMed ID: 36208099)
1. Identification and phenotypic analysis of novel LTBP2 mutations in a Chinese cohort with congenital ectopia lentis.
Liu L; Guo D; Yang F; Qi H; Zhou Y; Zheng D; Jin G
Mol Vis; 2023; 29():169-179. PubMed ID: 38222456
[TBL] [Abstract][Full Text] [Related]
2. Genotype-phenotype profile of global ASPH-associated ectopia lentis and clinical findings from a Chinese cohort.
Chen ZX; Jia WN; Sun Y; Jiang YX
Gene; 2024 May; 925():148600. PubMed ID: 38788814
[TBL] [Abstract][Full Text] [Related]
3. Compound heterozygous mutations in the LTBP2 gene associated with microspherophakia in a Chinese patient: a case report and literature review.
Xu M; Li K; He W
BMC Med Genomics; 2021 Sep; 14(1):227. PubMed ID: 34535142
[TBL] [Abstract][Full Text] [Related]
4. Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype-phenotype analysis of 105 patients.
Wang W; Gao SH; Wei M; Zhong LQ; Liu W; Jian S; Xiao J; Zhang CH; Zhang JG; Zeng XF; Xia WB; Qiu ZQ; Song HM
World J Pediatr; 2023 Jul; 19(7):674-686. PubMed ID: 36622578
[TBL] [Abstract][Full Text] [Related]
5. Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract.
Lecca M; Mauri L; Gana S; Del Longo A; Morelli F; Nicotra R; Plumari M; Galli J; Sirchia F; Valente EM; Cavallari U; Mazza M; Signorini S; Errichiello E
Clin Genet; 2024 Jun; ():. PubMed ID: 38840272
[TBL] [Abstract][Full Text] [Related]
6. Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysis.
Kanwar K; Bashey S; Bohnsack BL; Drackley A; Ing A; Rahmani S; Ranaivo HR; McMullen P; Skol A; Yap K; Allegretti V; Rossen JL
Am J Med Genet A; 2024 Apr; ():e63618. PubMed ID: 38597178
[TBL] [Abstract][Full Text] [Related]
7. [Ectopia lentis].
Britz L; Auffarth GU; Khoramnia R
Ophthalmologie; 2024 May; ():. PubMed ID: 38700761
[No Abstract] [Full Text] [Related]
8. Predicting axial length in patients with Marfan syndrome and ectopia lentis after modified capsular tension ring and intraocular lens implantation.
Chen ZX; Jia WN; Ma Y; Chen TH; Hong JH; Sun Y; Liu Y; Song LH; Jiang YX
J Cataract Refract Surg; 2023 Jun; 49(6):571-577. PubMed ID: 36745849
[TBL] [Abstract][Full Text] [Related]
9. A novel ADAMTSL4 compound heterozygous mutation in isolated ectopia lentis: a case report and review of the literature.
Wei H; Meng X; Qin H; Li X
J Med Case Rep; 2023 Dec; 17(1):532. PubMed ID: 38146062
[TBL] [Abstract][Full Text] [Related]
10. Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype-phenotype relationships.
Chen ZX; Jia WN; Sun Y; Chen TH; Zhao ZN; Lan LN; Liu Y; Song LH; Jiang YX
Hum Mutat; 2022 Dec; 43(12):2141-2152. PubMed ID: 36208099
[TBL] [Abstract][Full Text] [Related]
11. The phenotypic spectrum of
Knight LSW; Mullany S; Taranath DA; Ruddle JB; Barnett CP; Sallevelt SCEH; Berry EC; Marshall HN; Hollitt GL; Souzeau E; Craig JE; Siggs OM
Mol Vis; 2022; 28():257-268. PubMed ID: 36284667
[TBL] [Abstract][Full Text] [Related]
12. Novel
Guo D; Yang F; Zhou Y; Zhang X; Cao Q; Jin G; Zheng D
Br J Ophthalmol; 2023 Jun; 107(6):774-779. PubMed ID: 35042684
[TBL] [Abstract][Full Text] [Related]
13. Correlation between novel compound heterozygous ADAMTSL4 variants and primary phenotypes of ectopia lentis et pupillae.
Zhao J; Zhou Y; Zhang J; Zhang K; Shang L; Li J
Exp Eye Res; 2022 Nov; 224():109243. PubMed ID: 36089008
[TBL] [Abstract][Full Text] [Related]
14. A novel ADAMTSL4 mutation in autosomal recessive ectopia lentis et pupillae.
Christensen AE; Fiskerstrand T; Knappskog PM; Boman H; Rødahl E
Invest Ophthalmol Vis Sci; 2010 Dec; 51(12):6369-73. PubMed ID: 20702823
[TBL] [Abstract][Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]