BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

232 related articles for article (PubMed ID: 3893126)

  • 1. Prenatal diagnosis of Pena-Shokeir syndrome type 1.
    MacMillan RH; Harbert GM; Davis WD; Kelly TE
    Am J Med Genet; 1985 Jun; 21(2):279-84. PubMed ID: 3893126
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Antenatal diagnosis of Pena-Shokeir syndrome (type I) with ultrasonography and magnetic resonance imaging.
    Persutte WH; Lenke RR; Kurczynski TW; Brinker RA
    Obstet Gynecol; 1988 Sep; 72(3 Pt 2):472-5. PubMed ID: 3043297
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Sibs with the fetal akinesia sequence, fetal edema, and malformations: a new syndrome?
    Toriello HV; Bauserman SC; Higgins JV
    Am J Med Genet; 1985 Jun; 21(2):271-7. PubMed ID: 4040328
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Prenatal ultrasonographic features of the Pena-Shokeir I syndrome and the trisomy 18 syndrome.
    Muller LM; de Jong G
    Am J Med Genet; 1986 Sep; 25(1):119-29. PubMed ID: 3541607
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Prenatal diagnosis of Pena-Shokeir syndrome in the 27th week of pregnancy].
    Wieacker P; Wilhelm C; Böhm N; Schillinger H
    Geburtshilfe Frauenheilkd; 1990 Feb; 50(2):155-7. PubMed ID: 2180784
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Morphological study of the removed fetus after therapeutic abortion for echographic anomalies (apropos of 42 cases)].
    Serville F; Carles D; Mainguene M; Maugey B; Vanga A
    J Genet Hum; 1985 Sep; 33(3-4):301-12. PubMed ID: 3903051
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Pena-Shokeir syndrome: report of five cases and further delineation of the syndrome.
    Chen H; Blumberg B; Immken L; Lachman R; Rightmire D; Fowler M; Bachman R; Beemer FA
    Am J Med Genet; 1983 Oct; 16(2):213-24. PubMed ID: 6650566
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of retinal detachment in Walker-Warburg syndrome.
    Farrell SA; Toi A; Leadman ML; Davidson RG; Caco C
    Am J Med Genet; 1987 Nov; 28(3):619-24. PubMed ID: 3122570
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of Meckel syndrome: case reports and literature review.
    Johnson VP; Holzwarth DR
    Am J Med Genet; 1984 Aug; 18(4):699-711. PubMed ID: 6207728
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The Pena-Shokeir syndrome].
    Zeller R; Benz J
    Gynakol Rundsch; 1989; 29(3):148-52. PubMed ID: 2807025
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Absent fetal movement response with a blunted cardioacceleratory fetal response to external vibratory acoustic stimulation in a fetus with the Pena-Shokeir syndrome (fetal akinesia and hypokinesia sequence).
    Sherer DM; Sanko SR; Metlay LA; Woods JR
    Am J Perinatol; 1992 Jan; 9(1):1-4. PubMed ID: 1550625
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of Pena Shokeir phenotype.
    Hall JG
    Am J Med Genet; 1986 Sep; 25(1):99-117. PubMed ID: 3541610
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Pena-Shokeir syndrome type I--combination of polyhydramnios and pulmonary hypoplasia in fetal akinesia].
    Deli T; Kovács T
    Orv Hetil; 2010 Jun; 151(24):990-3. PubMed ID: 20519182
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A lethal autosomal recessive syndrome of multiple congenital contractures.
    Herva R; Leisti J; Kirkinen P; Seppänen U
    Am J Med Genet; 1985 Mar; 20(3):431-9. PubMed ID: 3993672
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Examination of the second-trimester fetus with severe oligohydramnios using transvaginal scanning.
    Benacerraf BR
    Obstet Gynecol; 1990 Mar; 75(3 Pt 2):491-3. PubMed ID: 2406666
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Neu-Laxova syndrome in female sibs: clinical and pathological features with prenatal diagnosis in the second sib.
    Tolmie JL; Mortimer G; Doyle D; McKenzie R; McLaurin J; Neilson JP
    Am J Med Genet; 1987 May; 27(1):175-82. PubMed ID: 3300330
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and fetal pathology in a Turkish family harboring a novel nonsense mutation in the lysosomal alpha-N-acetyl-neuraminidase (sialidase) gene.
    Sergi C; Penzel R; Uhl J; Zoubaa S; Dietrich H; Decker N; Rieger P; Kopitz J; Otto HF; Kiessling M; Cantz M
    Hum Genet; 2001 Oct; 109(4):421-8. PubMed ID: 11702224
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Prenatal diagnosis of skeletal dysplasia: case report of a fetus with multiple anomalies].
    Novakov Mikić A; Stojić S; Konstantinidis G; Ristivojević A; Krnojelac D
    Med Pregl; 2000; 53(3-4):197-201. PubMed ID: 10965689
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.