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 *

157 related articles for article (PubMed ID: 24096629)

  • 1. Congenital linear streaks on the face and neck and microphthalmia in an infant girl.
    Kluger N; Bouissou A; Tauzin L; Puechberty J; Dereure O
    Acta Derm Venereol; 2014 May; 94(3):342-3. PubMed ID: 24096629
    [No Abstract]   [Full Text] [Related]  

  • 2. Linear skin defects and microphthalmia.
    Durack A; Mehta SG; Allen LE; Ozanic Bulic S; Burrows NP
    Clin Exp Dermatol; 2018 Oct; 43(7):860-862. PubMed ID: 29896851
    [No Abstract]   [Full Text] [Related]  

  • 3. Microphthalmia with linear skin defects syndrome (MIDAS).
    Banganho D; Oliveira I; Machado C; Póvoas M
    BMJ Case Rep; 2019 Apr; 12(4):. PubMed ID: 31015240
    [No Abstract]   [Full Text] [Related]  

  • 4. [COX7B mutations in MIDAS syndrome or microphthalmia with linear skin defects (MLS)].
    Dereure O
    Ann Dermatol Venereol; 2013 May; 140(5):405-6. PubMed ID: 23663720
    [No Abstract]   [Full Text] [Related]  

  • 5. Microphthalmia with linear skin defects syndrome.
    García-Rabasco A; De-Unamuno B; Martínez F; Febrer-Bosch I; Alegre-de-Miquel V
    Pediatr Dermatol; 2013; 30(6):e230-1. PubMed ID: 22612277
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Microphthalmia with linear skin defects (MLS) syndrome: familial presentation.
    Kumar P; Rajab A
    Clin Exp Dermatol; 2018 Mar; 43(2):196-197. PubMed ID: 29023962
    [No Abstract]   [Full Text] [Related]  

  • 7. Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS).
    Kayserili H; Cox TC; Cox LL; Basaran S; Kiliç G; Ballabio A; Yüksel-Apak M
    J Med Genet; 2001 Jun; 38(6):411-7. PubMed ID: 11424926
    [No Abstract]   [Full Text] [Related]  

  • 8. Linear Skin Defects with Multiple Congenital Anomalies (LSDMCA): An Unconventional Mitochondrial Disorder.
    Indrieri A; Franco B
    Genes (Basel); 2021 Feb; 12(2):. PubMed ID: 33670341
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndrome.
    Vergult S; Leroy B; Claerhout I; Menten B
    Mol Vis; 2013; 19():311-8. PubMed ID: 23401659
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dermatoscopic aspects of the microphthalmia with linear skin defects (MLS) syndrome.
    Almeida HL; Rossi G; Abreu LB; Bergamaschi C; Silva AB; Kutsche K
    An Bras Dermatol; 2014; 89(1):180-1. PubMed ID: 24626674
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microphthalmia with linear skin defects: a case report and review.
    Sharma VM; Ruiz de Luzuriaga AM; Waggoner D; Greenwald M; Stein SL
    Pediatr Dermatol; 2008; 25(5):548-52. PubMed ID: 18950397
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical spectrum of females with HCCS mutation: from no clinical signs to a neonatal lethal form of the microphthalmia with linear skin defects (MLS) syndrome.
    van Rahden VA; Rau I; Fuchs S; Kosyna FK; de Almeida HL; Fryssira H; Isidor B; Jauch A; Joubert M; Lachmeijer AM; Zweier C; Moog U; Kutsche K
    Orphanet J Rare Dis; 2014 Apr; 9():53. PubMed ID: 24735900
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Microphthalmia and linear skin defects syndrome: Precise diagnosis guides prognosis.
    Satcher KG; Maegawa GHB; Schoch JJ
    Pediatr Dermatol; 2020 Jan; 37(1):217-218. PubMed ID: 31373408
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microphthalmia with Linear Skin Defects (MLS) associated with Autism Spectrum Disorder (ASD) in a patient with Familial 12.9Mb Terminal Xp deletion.
    Margari L; Colonna A; Craig F; Gentile M; Giannella G; Lamanna AL; Legrottaglie AR
    BMC Pediatr; 2014 Sep; 14():220. PubMed ID: 25182979
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome.
    van Rahden VA; Fernandez-Vizarra E; Alawi M; Brand K; Fellmann F; Horn D; Zeviani M; Kutsche K
    Am J Hum Genet; 2015 Apr; 96(4):640-50. PubMed ID: 25772934
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.
    Wimplinger I; Morleo M; Rosenberger G; Iaconis D; Orth U; Meinecke P; Lerer I; Ballabio A; Gal A; Franco B; Kutsche K
    Am J Hum Genet; 2006 Nov; 79(5):878-89. PubMed ID: 17033964
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A mosaic form of microphthalmia with linear skin defects.
    Prepeluh N; Korpar B; Zagorac A; Zagradišnik B; Golub A; Kokalj Vokač N
    BMC Pediatr; 2018 Aug; 18(1):254. PubMed ID: 30068298
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome.
    Zhu X; Dai FR; Wang J; Zhang Y; Tan ZP; Zhang Y
    Gene; 2015 Oct; 571(1):142-4. PubMed ID: 26196063
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Xp22.3 microdeletion in a 19-year-old girl with clinical features of MLS syndrome.
    Enright F; Campbell P; Stallings RL; Hall K; Green AJ; Sweeney E; Barnes L; Watson R
    Pediatr Dermatol; 2003; 20(2):153-7. PubMed ID: 12657015
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects.
    Lindor NM; Michels VV; Hoppe DA; Driscoll DJ; Leavitt JA; Dewald GW
    Am J Med Genet; 1992 Sep; 44(1):61-5. PubMed ID: 1519653
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.