Kallmann syndrome due to a translocation resulting in an X/Y fusion gene. [electronic resource]
Producer: 19930609Description: 337-40 p. digitalISSN:- 1061-4036
- Amino Acid Sequence
- Base Sequence
- Cloning, Molecular
- Exons
- Humans
- Introns
- Kallmann Syndrome -- genetics
- Male
- Molecular Sequence Data
- Oligodeoxyribonucleotides
- Polymerase Chain Reaction -- methods
- Recombination, Genetic
- Restriction Mapping
- Sequence Homology, Amino Acid
- Sequence Homology, Nucleic Acid
- Translocation, Genetic
- X Chromosome
- Y Chromosome
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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