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2. Environmental and parental risk factors for congenital solitary functioning kidney - a case-control study

6. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy

9. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

11. Deletions and loss-of-function variants in TP63 associated with orofacial clefting

12. The European Anorectal Malformation Network (ARM-Net) patient registry: 10-year review of clinical and surgical characteristics.

13. Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy

14. Maternal risk factors for posterior urethral valves

15. A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney

16. More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation

17. Genome-wide association study in patients with posterior urethral valves

21. Genome-wide association analyses identify variants in developmental genes associated with hypospadias

26. CDH12 as a Candidate Gene for Kidney Injury in Posterior Urethral Valve Cases: A Genome-wide Association Study Among Patients with Obstructive Uropathies

27. Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across different populations

29. SLC20A1Is Involved in Urinary Tract and Urorectal Development

31. Clinical Differentiation between a Normal Anus, Anterior Anus, Congenital Anal Stenosis, and Perineal Fistula: Definitions and Consequences—The ARM-Net Consortium Consensus.

32. Inter- and Intraobserver Variation in the Assessment of Preoperative Colostograms in Male Anorectal Malformations: An ARM-Net Consortium Survey

33. SLC20A1 Is Involved in Urinary Tract and Urorectal Development

35. A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies

37. The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene.

38. Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

41. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

42. Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations

43. Maternal risk factors involved in specific congenital anomalies of the kidney and urinary tract : A case-control study

44. AGORA, a data- and biobank for birth defects and childhood cancer

45. Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT

46. Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis

47. Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis

48. AGORA, a data- and biobank for birth defects and childhood cancer

49. Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT

50. Maternal risk factors involved in specific congenital anomalies of the kidney and urinary tract: A case-control study

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