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 *

107 related articles for article (PubMed ID: 9689998)

  • 21. The enigma of anencephaly and spina bifida.
    Corcoran R
    Midwife Health Visit Community Nurse; 1975 Jul; 11(7):211-3. PubMed ID: 1094246
    [No Abstract]   [Full Text] [Related]  

  • 22. Chromosomal abnormalities in fetuses with open neural tube defects: prenatal identification with ultrasound.
    Sepulveda W; Corral E; Ayala C; Be C; Gutierrez J; Vasquez P
    Ultrasound Obstet Gynecol; 2004 Apr; 23(4):352-6. PubMed ID: 15065184
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spina bifida cystica. Incidence of spina bifida occulta in parents and in controls.
    Lorber J; Levick K
    Arch Dis Child; 1967 Apr; 42(222):171-3. PubMed ID: 5337444
    [No Abstract]   [Full Text] [Related]  

  • 24. Letter: Offspring of parents with spina bifida occulta.
    Field B; Kerr C
    Lancet; 1975 Dec; 2(7947):1257. PubMed ID: 53742
    [No Abstract]   [Full Text] [Related]  

  • 25. [Association of cranial dysostosis, occult spina bifida and enuresis in the same family].
    SARROUY C; LEGEAIS G; RICHAUD ; SANPERE Z
    Pediatrie; 1959; 14():551-5. PubMed ID: 14441801
    [No Abstract]   [Full Text] [Related]  

  • 26. The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida.
    Jensen LE; Hoess K; Whitehead AS; Mitchell LE
    Birth Defects Res A Clin Mol Teratol; 2005 Jul; 73(7):512-6. PubMed ID: 15959877
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatally detected fetal myelomeningocele: is karyotype analysis warranted?
    Babcook CJ; Goldstein RB; Filly RA
    Radiology; 1995 Feb; 194(2):491-4. PubMed ID: 7824730
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Karyotypic changes in spina bifida].
    Maccani U
    Minerva Pediatr; 1967 Nov; 19(47):2103-4. PubMed ID: 4884970
    [No Abstract]   [Full Text] [Related]  

  • 29. Discussion: familial spina bifida.
    Smith DW
    Birth Defects Orig Artic Ser; 1974; 10(7):23. PubMed ID: 4609332
    [No Abstract]   [Full Text] [Related]  

  • 30. Prenatal diagnosis and genetic counseling in a case of spina bifida in a family with Waardenburg syndrome type I.
    Kujat A; Veith VP; Faber R; Froster UG
    Fetal Diagn Ther; 2007; 22(2):155-8. PubMed ID: 17139175
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Diagnosis of spina bifida on ultrasound: always termination?
    Trudell AS; Odibo AO
    Best Pract Res Clin Obstet Gynaecol; 2014 Apr; 28(3):367-77. PubMed ID: 24373566
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Trisomy 13 ascertained in a survey of spontaneous abortions.
    Jacobs PA; Hassold TJ; Henry A; Pettay D; Takaesu N
    J Med Genet; 1987 Dec; 24(12):721-4. PubMed ID: 3430552
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mechanisms of mutant genes in spina bifida: a review of implications from animal models.
    George TM; McLone DG
    Pediatr Neurosurg; 1995; 23(5):236-45. PubMed ID: 8688348
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Origin of acrocentric trisomies in spontaneous abortuses.
    Niikawa N; Merotto E; Kajii T
    Hum Genet; 1977 Dec; 40(1):73-8. PubMed ID: 604246
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A genetic study of spina bifida cystica in Utah.
    Woolf CM
    Soc Biol; 1975; 22(3):216-20. PubMed ID: 766191
    [No Abstract]   [Full Text] [Related]  

  • 36. Letter: Anencephaly, spina bifida, dizygotic twinning, and hormones.
    James WH
    Lancet; 1974 May; 1(7864):1007. PubMed ID: 4133639
    [No Abstract]   [Full Text] [Related]  

  • 37. [Prenatal ultrasound findings in complete trisomy 9].
    Borowski D; Hincz P; Wyrwas D; Kunert A; Szaflik K; Ałaszewski W; Grzesiak M; Jakubowski L; Bielak A; Wilczyński J
    Ginekol Pol; 2006 May; 77(5):394-7. PubMed ID: 16958230
    [TBL] [Abstract][Full Text] [Related]  

  • 38. C677T mutation in methylenetetrahydrofolate reductase gene and neural tube defects: should Japanese women undergo gene screening before pregnancy?
    Kondo A; Fukuda H; Matsuo T; Shinozaki K; Okai I
    Congenit Anom (Kyoto); 2014 Feb; 54(1):30-4. PubMed ID: 24588777
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Protein kinase profiling in miscarriage: implications for the pathogenesis of trisomic pregnancy.
    Yong PJ; McFadden DE; Robinson WP
    J Obstet Gynaecol Can; 2012 Dec; 34(12):1141-1148. PubMed ID: 23231796
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Spina bifida].
    Mühl-Benninghaus R
    Radiologe; 2018 Jul; 58(7):659-663. PubMed ID: 29797041
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.