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1. Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies

2. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

3. Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital abnormalities

4. Variants in genes coding for collagen type IV [alpha]-chains are frequent causes of persistent, isolated hematuria during childhood

5. DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.

6. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

7. Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies

8. Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene

10. List of contributors

11. Rare variants inPPFIA3cause delayed development, intellectual disability, autism, and epilepsy

12. Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes

13. Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

16. Variants in genes coding for collagen type IV α-chains are frequent causes of persistent, isolated hematuria during childhood.

17. Mutations of the histone linker H1–4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4

24. Characterization of the renal phenotype in RMND1 ‐related mitochondrial disease

25. DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

26. Nephronophthisis due to a novel DCDC2 variant in a patient from African‐Caribbean descent: A case report.

27. Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy.

28. Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases.

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