Lack of LGR8 gene mutation in Finnish patients with a family history of cryptorchidism. [electronic resource]
Producer: 20040625Description: 400-6 p. digitalISSN:- 1472-6483
- Adult
- Alleles
- Cell Line
- Cryptorchidism -- genetics
- Cyclic AMP -- metabolism
- DNA -- chemistry
- DNA, Complementary -- metabolism
- Dose-Response Relationship, Drug
- Exons
- Family Health
- Fathers
- Female
- Finland
- Genetic Variation
- Heterozygote
- Homozygote
- Humans
- Introns
- Male
- Mothers
- Mutation
- Polymerase Chain Reaction
- Polymorphism, Genetic
- Receptors, G-Protein-Coupled
- Receptors, Peptide -- genetics
- Sequence Analysis, DNA
- Signal Transduction
- Transfection
- Valine -- chemistry
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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