BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 27430178)

  • 1. Prenatal Detection of Peters' Plus Syndrome in a Patient with No Known Family History.
    Shima Y; Migita M
    J Nippon Med Sch; 2016; 83(3):130-2. PubMed ID: 27430178
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hydrocephalus, agenesis of the corpus callosum, and cleft lip/palate represent frequent associations in fetuses with Peters' plus syndrome and B3GALTL mutations. Fetal PPS phenotypes, expanded by Dandy Walker cyst and encephalocele.
    Schoner K; Kohlhase J; Müller AM; Schramm T; Plassmann M; Schmitz R; Neesen J; Wieacker P; Rehder H
    Prenat Diagn; 2013 Jan; 33(1):75-80. PubMed ID: 23161355
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Severe Peters Plus syndrome-like phenotype with anterior eye staphyloma and hypoplastic left heart syndrome: proposal of a new syndrome.
    Shimizu R; Saito R; Hoshino K; Ogawa K; Negishi T; Nishimura J; Mitsui N; Osawa M; Ohashi H
    Congenit Anom (Kyoto); 2010 Sep; 50(3):197-9. PubMed ID: 20584037
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mobile Retrolental Cyst in a Child With Peters Plus Syndrome.
    Cavuoto KM; Chang TC
    JAMA Ophthalmol; 2016 Oct; 134(10):e162125. PubMed ID: 27737454
    [No Abstract]   [Full Text] [Related]  

  • 5. Unique Presentation of Corneal Opacity in Peters Plus Syndrome: An Unusual Form of Peters Anomaly Showing Tissue Repair in Serial Analysis.
    de Nie KF; Wesseling P; Eggink CA
    Cornea; 2016 Feb; 35(2):277-80. PubMed ID: 26684045
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ocular Phenotype of Peters-Plus Syndrome.
    Shah PR; Chauhan B; Chu CT; Kofler J; Nischal KK
    Cornea; 2022 Feb; 41(2):219-223. PubMed ID: 34629439
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole-exome sequencing for diagnosis of Peters-plus syndrome after prenatal diagnosis of recurrent low PAPP-A and multiple fetal anomalies in two consecutive pregnancies.
    Kamalapathy P; Fonda Allen JS; Macri CJ; Lawrence AK; Regier DS; Rubio EI
    J Neonatal Perinatal Med; 2019; 12(3):333-338. PubMed ID: 31476172
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Peters plus syndrome and Chorioretinal findings associated with B3GLCT gene mutation - a case report.
    Wang YE; Ramirez DA; Chang TC; Berrocal A
    BMC Ophthalmol; 2020 Mar; 20(1):118. PubMed ID: 32204707
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Peters Plus syndrome: a recognizable clinical entity.
    Demir GÜ; Lafcı NG; Doğan ÖA; Şimşek-Kiper PÖ; Utine GE
    Turk J Pediatr; 2020; 62(1):136-140. PubMed ID: 32253880
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical utility gene card for: Peters plus syndrome.
    Jaeken J; Lefeber DJ; Matthijs G
    Eur J Hum Genet; 2016 Aug; 24(8):. PubMed ID: 27049305
    [No Abstract]   [Full Text] [Related]  

  • 11. Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.
    de Almeida JC; Reis DF; Llerena Júnior J; Barbosa Neto J; Pontes RL; Middleton S; Telles LF
    J Med Genet; 1991 Apr; 28(4):277-9. PubMed ID: 1856836
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Contribution of a Novel
    Totoń-Żurańska J; Kapusta P; Rybak-Krzyszkowska M; Lorenc K; Machlowska J; Skalniak A; Filipek E; Pawlik D; Wołkow PP
    Int J Mol Sci; 2019 Nov; 20(23):. PubMed ID: 31795264
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Peters'-Plus syndrome: report on an unusual case.
    Camera G; Pozzolo S; Carta M; Righi E
    Pathologica; 1994 Dec; 86(6):673-5. PubMed ID: 7617402
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Peters' anomaly. The spectrum of associated ocular and systemic malformations.
    Heon E; Barsoum-Homsy M; Cevrette L; Jacob JL; Milot J; Polemeno R; Musarella MA
    Ophthalmic Paediatr Genet; 1992 Jun; 13(2):137-43. PubMed ID: 1495764
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Peters' anomaly as a consequence of genetic and nongenetic syndromes.
    Kivlin JD; Fineman RM; Crandall AS; Olson RJ
    Arch Ophthalmol; 1986 Jan; 104(1):61-4. PubMed ID: 3079999
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Nasal dermoid sinus cyst: accidental coincidence or syndrome association?].
    Pausch NC; Frerich B; Hemprich A; Brylla E; Sterker I; Merkenschlager A
    Klin Padiatr; 2008; 220(5):321-4. PubMed ID: 18401812
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Peters-plus syndrome: Report of a rare case].
    Moutei H; Bennis A; Chraibi F; Abdellaoui M; Benatiya IA
    J Fr Ophtalmol; 2021 Jan; 44(1):115-116. PubMed ID: 33268148
    [No Abstract]   [Full Text] [Related]  

  • 18. Vertebral defects in patients with Peters plus syndrome and mutations in B3GALTL.
    Faletra F; Athanasakis E; Minen F; Fornasier F; Marchetti F; Gasparini P
    Ophthalmic Genet; 2011 Nov; 32(4):256-8. PubMed ID: 21671750
    [No Abstract]   [Full Text] [Related]  

  • 19. Peters' plus syndrome.
    de Almeida JC; Llerena Júnior JC
    Am J Med Genet; 1993 Aug; 47(1):125. PubMed ID: 8368243
    [No Abstract]   [Full Text] [Related]  

  • 20. The Peters' plus syndrome: a review.
    Maillette de Buy Wenniger-Prick LJ; Hennekam RC
    Ann Genet; 2002; 45(2):97-103. PubMed ID: 12119218
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.