BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 26429400)

  • 41. A 17q12 chromosomal duplication associated with renal disease and esophageal atresia.
    Faguer S; Chassaing N; Bandin F; Prouheze C; Arveiler B; Rooryck C; Nogier MB; Chauveau D; Calvas P; Decramer S
    Eur J Med Genet; 2011; 54(4):e437-40. PubMed ID: 21540130
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 17q12 Deletion Syndrome as a Rare Cause for Diabetes Mellitus Type MODY5.
    Roehlen N; Hilger H; Stock F; Gläser B; Guhl J; Schmitt-Graeff A; Seufert J; Laubner K
    J Clin Endocrinol Metab; 2018 Oct; 103(10):3601-3610. PubMed ID: 30032214
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries.
    Wiesel A; Queisser-Luft A; Clementi M; Bianca S; Stoll C;
    Eur J Med Genet; 2005; 48(2):131-44. PubMed ID: 16053904
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Prenatal ultrasound findings of lissencephaly associated with Miller-Dieker syndrome and comparison with pre- and postnatal magnetic resonance imaging.
    Fong KW; Ghai S; Toi A; Blaser S; Winsor EJ; Chitayat D
    Ultrasound Obstet Gynecol; 2004 Dec; 24(7):716-23. PubMed ID: 15586369
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.
    Bretelle F; Beyer L; Pellissier MC; Missirian C; Sigaudy S; Gamerre M; D'Ercole C; Philip N
    Eur J Med Genet; 2010; 53(6):367-70. PubMed ID: 20659598
    [TBL] [Abstract][Full Text] [Related]  

  • 46. TCF2/HNF-1beta mutations: 3 cases of fetal severe pancreatic agenesis or hypoplasia and multicystic renal dysplasia.
    Body-Bechou D; Loget P; D'Herve D; Le Fiblec B; Grebille AG; Le Guern H; Labarthe C; Redpath M; Cabaret-Dufour AS; Sylvie O; Fievet A; Antignac C; Heidet L; Taque S; Patrice P
    Prenat Diagn; 2014 Jan; 34(1):90-3. PubMed ID: 24382792
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Concurrent of compound heterozygous variant of a novel in-frame deletion and the common hypomorphic haplotype in TBX6 and inherited 17q12 microdeletion in a fetus.
    Li G; Chen Y; Han X; Li N; Li S
    BMC Pregnancy Childbirth; 2024 Jul; 24(1):456. PubMed ID: 38951757
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Imperforate anus: A relatively common anomaly rarely diagnosed prenatally.
    Brantberg A; Blaas HG; Haugen SE; Isaksen CV; Eik-Nes SH
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):904-10. PubMed ID: 17091530
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene.
    Tse WT; Cao Y; Lam PPH; Law KM; Choy KW; Ting YH
    Prenat Diagn; 2024 Feb; 44(2):251-254. PubMed ID: 38141042
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Ultrasound diagnosis of fetal renal abnormalities.
    Dias T; Sairam S; Kumarasiri S
    Best Pract Res Clin Obstet Gynaecol; 2014 Apr; 28(3):403-15. PubMed ID: 24524801
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and management.
    Aubertin G; Cripps S; Coleman G; McGillivray B; Yong SL; Van Allen M; Shaw D; Arbour L
    Prenat Diagn; 2002 May; 22(5):388-94. PubMed ID: 12001193
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Prenatal diagnosis of renal anomalies.
    Kaffe S; Rose JS; Godmilow L; Walker BA; Kerenyi T; Beratis N; Reyes P; Hirschhorn K
    Am J Med Genet; 1977; 1(2):241-51. PubMed ID: 610432
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Correlation between ultrasound and anatomical findings in fetuses with lower urinary tract obstruction in the first half of pregnancy.
    Robyr R; Benachi A; Daikha-Dahmane F; Martinovich J; Dumez Y; Ville Y
    Ultrasound Obstet Gynecol; 2005 May; 25(5):478-82. PubMed ID: 15816021
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Increased renal parenchymal echogenicity in the fetus: importance and clinical outcome.
    Estroff JA; Mandell J; Benacerraf BR
    Radiology; 1991 Oct; 181(1):135-9. PubMed ID: 1887022
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Increased incidence of renal anomalies in patients with chromosome 22q11 microdeletion.
    Stewart TL; Irons MB; Cowan JM; Bianchi DW
    Teratology; 1999 Jan; 59(1):20-2. PubMed ID: 9988879
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 17q12 microdeletion syndrome: three patients illustrating the phenotypic spectrum.
    Dixit A; Patel C; Harrison R; Jarvis J; Hulton S; Smith N; Yates K; Silcock L; McMullan DJ; Suri M
    Am J Med Genet A; 2012 Sep; 158A(9):2317-21. PubMed ID: 22887843
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Severe neonatal presentation of Kleefstra syndrome in a patient with hypoplastic left heart syndrome and 9q34.3 microdeletion.
    Campbell CL; Collins RT; Zarate YA
    Birth Defects Res A Clin Mol Teratol; 2014 Dec; 100(12):985-90. PubMed ID: 25380126
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4.
    Molin A; Benoist G; Jeanne-Pasquier C; Elkartoufi N; Litzer J; Decamp M; Gruchy N; Durand-Malbruny M; Begorre M; Attie-Bitach T; Leporrier N
    Eur J Med Genet; 2013 Oct; 56(10):580-3. PubMed ID: 23954617
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Genetic syndromes and prenatally detected renal anomalies.
    Deshpande C; Hennekam RC
    Semin Fetal Neonatal Med; 2008 Jun; 13(3):171-80. PubMed ID: 18162447
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome presenting with a large nephrogenic cyst, severe oligohydramnios and hydrops fetalis: a case report and review of the literature.
    Chuangsuwanich T; Sunsaneevithayakul P; Muangsomboon K; Limwongse C
    Prenat Diagn; 2005 Mar; 25(3):210-5. PubMed ID: 15791665
    [TBL] [Abstract][Full Text] [Related]  

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