Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13)-Reference-Cited by-同舟云学术

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Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13)

Published:1993-02-01 Issue:3 Volume:45 Page:335-339
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Chen Harold,Aiello Frank

Publisher

Wiley

Subject

Genetics(clinical)

Reference41 articles.

1. TRIMETHYLAMINURIA (FISH-ODOUR SYNDROME): AN INBORN ERROR OF OXIDATIVE METABOLISM

2. A Genetic polymorphism of the N-oxidation of trimethylamine in humans

3. Trimethylaminuria (‘fish-odour syndrome’): A study of an affected family

4. Trimethylaminuria: The detection of carriers using a trimethylamine load test

Cited by 12 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. Trimethylaminuria;Atlas of Genetic Diagnosis and Counseling;2017

2. Trimethylaminuria;Atlas of Genetic Diagnosis and Counseling;2016

3. Fish Malodour syndrome in a child;Case Reports;2015-04-13

4. Trimethylaminuria (fish odor syndrome): Genotype characterization among Portuguese patients;Gene;2013-09

5. Trimethylaminuria;Atlas of Genetic Diagnosis and Counseling;2012

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