Found: 3
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The Importance of the α<sub>2</sub>MR/LRP for Human Genetics.
- Published in:
- Annals of the New York Academy of Sciences, 1994, v. 737, n. 1, p. 447, doi. 10.1111/j.1749-6632.1994.tb44336.x
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- Article
Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 2, p. 223, doi. 10.1093/hmg/5.2.223
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- Publication type:
- Article
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 3, p. 323
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- Article