BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 7479596)

  • 21. Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus.
    Lin CY; Chen CP; Liau CL; Su PH; Tsao TF; Chang TY; Wang W
    Taiwan J Obstet Gynecol; 2009 Dec; 48(4):408-11. PubMed ID: 20045764
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk population.
    Drummond CL; Gomes DM; Senat MV; Audibert F; Dorion A; Ville Y
    Prenat Diagn; 2003 Dec; 23(13):1068-72. PubMed ID: 14691994
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Heterogeneity in fetal akinesia deformation sequence (FADS): autopsy confirmation in three 20-21-week fetuses.
    Yfantis H; Nonaka D; Castellani R; Harman C; Sun CC
    Prenat Diagn; 2002 Jan; 22(1):42-7. PubMed ID: 11810649
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal features of Pena-Shokeir sequence with atypical response to acoustic stimulation.
    Pittyanont S; Jatavan P; Suwansirikul S; Tongsong T
    J Clin Ultrasound; 2016 Sep; 44(7):459-62. PubMed ID: 27312123
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review.
    Chen CP
    Taiwan J Obstet Gynecol; 2012 Mar; 51(1):12-7. PubMed ID: 22482962
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal ultrasonographic diagnosis of the cerebro-costo-mandibular syndrome: case report and review of the literature.
    Megier P; Ayeva-Derman M; Esperandieu O; Aubry MC; Couly G; Desroches A
    Prenat Diagn; 1998 Dec; 18(12):1294-9. PubMed ID: 9885022
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The application of three-dimensional ultrasonography in the prenatal diagnosis of arthrogryposis.
    Lin IW; Chueh HY; Chang SD; Cheng PJ
    Taiwan J Obstet Gynecol; 2008 Mar; 47(1):75-8. PubMed ID: 18400586
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fetal ultrasound.
    Kennedy A
    Curr Probl Diagn Radiol; 2000; 29(4):109-40. PubMed ID: 10914314
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cerebro-costo-mandibular syndrome: early sonographic prenatal diagnosis.
    Ibba RM; Corda A; Zoppi MA; Floris M; Todde P; Monni G
    Ultrasound Obstet Gynecol; 1997 Aug; 10(2):142-4. PubMed ID: 9286027
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Pena-Shokeir phenotype (fetal akinesia/hypokinesia sequence)].
    Dzinović A; Heljić S
    Med Arh; 2006; 60(6):383-5. PubMed ID: 17297855
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal sonographic diagnosis of Pena-Shokeir syndrome type I, or fetal akinesia deformation sequence.
    Ohlsson A; Fong KW; Rose TH; Moore DC
    Am J Med Genet; 1988 Jan; 29(1):59-65. PubMed ID: 3278614
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Pena-Shokeir syndrome: report of a case with benign outcome].
    Romeo MG; Betta P; Rodonò A; Tina LG; Distefano G
    Pediatr Med Chir; 1995; 17(1):73-5. PubMed ID: 7739933
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Arthrogryposis multiplex congenita, Pena-Shokeir phenotype, with gastroschisis and agenesis of the leg.
    Agapitos M; Georgiou-Theodoropoulou M; Koutselinis A; Papacharalambus N
    Pediatr Pathol; 1988; 8(4):409-13. PubMed ID: 2974953
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Serial postural and motor assessment of Fetal Akinesia Deformation Sequence (FADS).
    Donker ME; Eijckelhof BH; Tan GM; de Vries JI
    Early Hum Dev; 2009 Dec; 85(12):785-90. PubMed ID: 19944545
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pena-Shokeir phenotype in sibs with macrocephaly but without growth retardation.
    Lammer EJ; Donnelly S; Holmes LB
    Am J Med Genet; 1989 Apr; 32(4):478-81. PubMed ID: 2672815
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hypoechogenicity of fetal long bones: a new ultrasound marker for arthrogryposis.
    Murphy JC; Neale D; Bromley B; Benacerraf BR; Copel JA
    Prenat Diagn; 2002 Dec; 22(13):1219-22. PubMed ID: 12478637
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Disturbances in neuronal migration and laminar cortical organization associated with multicystic encephalopathy in the Pena-Shokeir syndrome.
    Choi BH; Ruess WR; Kim RC
    Acta Neuropathol; 1986; 69(3-4):177-83. PubMed ID: 3754373
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Fetal akinesia deformation sequence. Pena-Shokeir type I syndrome: new features of an un-uncommon condition.
    Eguiluz I; Barber MA; Martín A; Plasencia W; Arencibia O
    J Obstet Gynaecol; 2006 Nov; 26(8):818-20. PubMed ID: 17130047
    [No Abstract]   [Full Text] [Related]  

  • 39. Visual diagnosis in utero: Prenatal diagnosis of Treacher-Collins syndrome using a 3D/4D ultrasonography.
    Kubo S; Horinouchi T; Kinoshita M; Yoshizato T; Kozuma Y; Shinagawa T; Ushijima K
    Taiwan J Obstet Gynecol; 2019 Jul; 58(4):566-569. PubMed ID: 31307753
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Polyhydramnios, fetal overgrowth, and macrocephaly: prenatal ultrasound findings of Costello syndrome.
    Smith LP; Podraza J; Proud VK
    Am J Med Genet A; 2009 Feb; 149A(4):779-84. PubMed ID: 19288554
    [TBL] [Abstract][Full Text] [Related]  

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