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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

318 related items for PubMed ID: 19668217

  • 21. Foxc1 dependent mesenchymal signalling drives embryonic cerebellar growth.
    Haldipur P, Gillies GS, Janson OK, Chizhikov VV, Mithal DS, Miller RJ, Millen KJ.
    Elife; 2014 Dec 16; 3():. PubMed ID: 25513817
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Enlarged cisterna magna and the Dandy-Walker malformation: factors associated with chromosome abnormalities.
    Nyberg DA, Mahony BS, Hegge FN, Hickok D, Luthy DA, Kapur R.
    Obstet Gynecol; 1991 Mar 16; 77(3):436-42. PubMed ID: 1992413
    [Abstract] [Full Text] [Related]

  • 24. Outcome of fetal cerebral posterior fossa anomalies.
    Long A, Moran P, Robson S.
    Prenat Diagn; 2006 Aug 16; 26(8):707-10. PubMed ID: 16764010
    [Abstract] [Full Text] [Related]

  • 25. Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions.
    Ferraris A, Bernardini L, Sabolic Avramovska V, Zanni G, Loddo S, Sukarova-Angelovska E, Parisi V, Capalbo A, Tumini S, Travaglini L, Mancini F, Duma F, Barresi S, Novelli A, Mercuri E, Tarani L, Italian CBCD Study Group, Bertini E, Dallapiccola B, Valente EM.
    Orphanet J Rare Dis; 2013 May 16; 8():75. PubMed ID: 23679990
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Prenatal diagnosis of Dandy-Walker malformation: report of a case.
    Chen FP, Chu KK.
    J Formos Med Assoc; 1994 May 16; 93(11-12):967-70. PubMed ID: 7633204
    [Abstract] [Full Text] [Related]

  • 28. Multiple congenital malformations including severe eye anomalies and abnormal cerebellar development with Dandy-Walker malformation in a girl with partial trisomy 3q.
    de Azevedo Moreira LM, Neri FB, de Quadros Uzeda S, de Carvalho AF, Santana GC, Souza FR, Rollemberg JC.
    Ophthalmic Genet; 2005 Mar 16; 26(1):37-43. PubMed ID: 15823924
    [Abstract] [Full Text] [Related]

  • 29. A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye.
    Nishimura DY, Searby CC, Alward WL, Walton D, Craig JE, Mackey DA, Kawase K, Kanis AB, Patil SR, Stone EM, Sheffield VC.
    Am J Hum Genet; 2001 Feb 16; 68(2):364-72. PubMed ID: 11170889
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Fetal and neonatal outcomes of posterior fossa anomalies: a retrospective cohort study.
    Alsehli H, Alshahrani SM, Alzahrani S, Ababneh F, Alharbi NM, Alarfaj N, Baarmah D.
    Sci Rep; 2024 Apr 10; 14(1):8411. PubMed ID: 38600369
    [Abstract] [Full Text] [Related]

  • 35. Anirdia-like phenotype caused by 6p25 dosage aberrations.
    Sadagopan KA, Liu GT, Capasso JE, Wuthisiri W, Keep RB, Levin AV.
    Am J Med Genet A; 2015 Mar 10; 167A(3):524-8. PubMed ID: 25691405
    [Abstract] [Full Text] [Related]

  • 36. Blake's Pouch Cysts and Differential Diagnoses in Prenatal and Postnatal MRI : A Pictorial Review.
    Kau T, Marterer R, Kottke R, Birnbacher R, Gellen J, Nagy E, Boltshauser E.
    Clin Neuroradiol; 2020 Sep 10; 30(3):435-445. PubMed ID: 31942658
    [Abstract] [Full Text] [Related]

  • 37. Axenfeld-Rieger anomaly and Axenfeld-Rieger syndrome: clinical, molecular-cytogenetic, and DNA array analyses of three patients with chromosomal defects at 6p25.
    Tonoki H, Harada N, Shimokawa O, Yosozumi A, Monzaki K, Satoh K, Kosaki R, Sato A, Matsumoto N, Iizuka S.
    Am J Med Genet A; 2011 Dec 10; 155A(12):2925-32. PubMed ID: 22009788
    [Abstract] [Full Text] [Related]

  • 38. Hindbrain morphometry and choroid plexus position in differential diagnosis of posterior fossa cystic malformations.
    Paladini D, Donarini G, Parodi S, Volpe G, Sglavo G, Fulcheri E.
    Ultrasound Obstet Gynecol; 2019 Aug 10; 54(2):207-214. PubMed ID: 30207001
    [Abstract] [Full Text] [Related]

  • 39. Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.
    Strungaru MH, Dinu I, Walter MA.
    Invest Ophthalmol Vis Sci; 2007 Jan 10; 48(1):228-37. PubMed ID: 17197537
    [Abstract] [Full Text] [Related]

  • 40. X-linked inheritance of Dandy-Walker variant.
    Wakeling EL, Jolly M, Fisk NM, Gannon C, Holder SE.
    Clin Dysmorphol; 2002 Jan 10; 11(1):15-8. PubMed ID: 11822699
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 16.