KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Molecular Biology,Biochemistry
Reference22 articles.
1. Sex and smell – an enigma resolved
2. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
3. Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway.
4. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
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