These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 1519650)

  • 21. Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome.
    Faivre L; Dollfus H; Lyonnet S; Alembik Y; Mégarbané A; Samples J; Gorlin RJ; Alswaid A; Feingold J; Le Merrer M; Munnich A; Cormier-Daire V
    Am J Med Genet A; 2003 Dec; 123A(2):204-7. PubMed ID: 14598350
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Autosomal dominant Weill-Marchesani syndrome and glaucoma management.
    Saricaoglu MS; Sengun A; Karakurt A; Colluoglu Z
    Saudi Med J; 2005 Sep; 26(9):1468-9. PubMed ID: 16155673
    [No Abstract]   [Full Text] [Related]  

  • 23. New syndrome: familial proportionate short stature, intrauterine growth retardation, and recurrent locking of the fingers.
    Eng CE; Strom CM
    Am J Med Genet; 1987 Jan; 26(1):217-20. PubMed ID: 3812565
    [No Abstract]   [Full Text] [Related]  

  • 24. [The Weill-Marchesani syndrome in a mother and son--its evolution with time].
    Iordănescu C; Banciu L; Tudor EP; Stamate E
    Oftalmologia; 1991; 35(1):57-60. PubMed ID: 1811740
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetics of ectopia lentis.
    Sadiq MA; Vanderveen D
    Semin Ophthalmol; 2013; 28(5-6):313-20. PubMed ID: 24138040
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Acute angle-closure glaucoma in a highly myopic patient secondary to Weill-Marchesani syndrome: histopathologic lens features.
    Lim SH; Son JH; Cha SC
    Int Ophthalmol; 2016 Dec; 36(6):921-924. PubMed ID: 26966104
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Similarity of geleophysic dysplasia and Weill-Marchesani syndrome.
    Kochhar A; Kirmani S; Cetta F; Younge B; Hyland JC; Michels V
    Am J Med Genet A; 2013 Dec; 161A(12):3130-2. PubMed ID: 24214363
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Anesthetic management of a patient with Weill-Marchesani syndrome.
    Dal D; Sahin A; Aypar U
    Acta Anaesthesiol Scand; 2003 Mar; 47(3):369-70. PubMed ID: 12648208
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Weill-Marchesani Syndrome, a Rare Presentation of Severe Short Stature with Review of the Literature.
    Al Motawa MNA; Al Shehri MSS; Al Buali MJ; Al Agnam AAM
    Am J Case Rep; 2021 May; 22():e930824. PubMed ID: 34057920
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Differential diagnosis and treatment of dislocated lenses.
    Cross HE
    Birth Defects Orig Artic Ser; 1976; 12(3):335-46. PubMed ID: 953198
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Characteristics and genotype-phenotype correlations in ADAMTS17 mutation-related Weill-Marchesani syndrome.
    Guo D; Liu L; Yang F; Young CA; Zheng D; Jin G
    Exp Eye Res; 2023 Sep; 234():109606. PubMed ID: 37506754
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A Pedigree Report of a Rare Case of Weill-Marchesani Syndrome with New Compound Heterozygous LTBP2 Mutations.
    Lin Z; Zhu M; Deng H
    Risk Manag Healthc Policy; 2021; 14():1785-1789. PubMed ID: 33958902
    [TBL] [Abstract][Full Text] [Related]  

  • 33. In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome.
    Faivre L; Gorlin RJ; Wirtz MK; Godfrey M; Dagoneau N; Samples JR; Le Merrer M; Collod-Beroud G; Boileau C; Munnich A; Cormier-Daire V
    J Med Genet; 2003 Jan; 40(1):34-6. PubMed ID: 12525539
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Evaluation of surgical intervention in familial isolated simple ectopia lentis: younger v. older generations.
    Galvin JA; Baker JD; Bawle EV
    Binocul Vis Strabismus Q; 2002; 17(3):229-34. PubMed ID: 12171597
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Sibs with growth deficiency, delayed bone age, congenital hip dislocation, and iridocorneal abnormalities with glaucoma.
    Stratton RF; Parker MW; McKeown CA; Johnson CP
    Am J Med Genet; 1989 Mar; 32(3):330-2. PubMed ID: 2729352
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Anesthetic characteristics and airway evaluation of patients with Weill-Marchesani syndrome.
    Riad W; Abouammoh M; Fathy M
    Middle East J Anaesthesiol; 2006 Feb; 18(4):725-31. PubMed ID: 16749567
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral ectopia lentis.
    Greene VB; Stoetzel C; Pelletier V; Perdomo-Trujillo Y; Liebermann L; Marion V; De Korvin H; Boileau C; Dufier JL; Dollfus H
    Ophthalmic Genet; 2010 Mar; 31(1):47-51. PubMed ID: 20141359
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Weill-Marchesani syndrome associated with retinitis pigmentosa.
    Jethani J; Mishra A; Shetty S; Vijayalakshmi P
    Indian J Ophthalmol; 2007; 55(2):142-3. PubMed ID: 17322607
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fibrillin-1 Gene Variant p.Gly1754Ser Associated With Weill-Marchesani Syndrome Type 2: A Case Report.
    Tamhankar PM; Menon P; Mane SV; Muthu Kumar A
    Cureus; 2024 Sep; 16(9):e69448. PubMed ID: 39421111
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hereditary ectopia lentis. A series of 10 cases of ectopia lentis et pupillae.
    Meire FM
    Bull Soc Belge Ophtalmol; 1991; 241():25-36. PubMed ID: 1840993
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.