Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease-Reference-Cited by-同舟云学术

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Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease

Published:2003-02-01 Issue:2 Volume:40 Page:17e-17
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:
Short-container-title:

Author:

Smulders Y M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. TFE3‐rearranged nonmelanotic renal PEComa: a case series expanding their phenotypic and fusion landscape;Histopathology;2024-08-21

2. TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant;Nefrología;2020-01

3. TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant;Nefrología (English Edition);2020-01

4. Evolution and Embryonic Development;Evolution's Clinical Guidebook;2019

5. Diagnosis of tuberous sclerosis complex in the fetus;European Journal of Paediatric Neurology;2018-11

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