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109 results
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Fraser syndrome: diagnosed in a 50-year-old museum specimen.
El├žioglu HN, Berry AC. El├žioglu HN, et al. Among authors: berry ac. Am J Med Genet. 2000 Sep 18;94(3):262-4. doi: 10.1002/1096-8628(20000918)94:3<262::aid-ajmg14>3.0.co;2-9. Am J Med Genet. 2000. PMID: 10995515 No abstract available.
Rubinstein-Taybi syndrome.
Berry AC. Berry AC. J Med Genet. 1987 Sep;24(9):562-6. doi: 10.1136/jmg.24.9.562. J Med Genet. 1987. PMID: 3312608 Free PMC article. Review. No abstract available.
A new form of autosomal dominant arthrogryposis.
Lai MM, Tettenborn MA, Hall JG, Smith LJ, Berry AC. Lai MM, et al. Among authors: berry ac. J Med Genet. 1991 Oct;28(10):701-3. doi: 10.1136/jmg.28.10.701. J Med Genet. 1991. PMID: 1941966 Free PMC article.
Chondrodysplasia punctata: another possible X-linked recessive case.
Bennett CP, Berry AC, Maxwell DJ, Seller MJ. Bennett CP, et al. Among authors: berry ac. Am J Med Genet. 1992 Dec 1;44(6):795-9. doi: 10.1002/ajmg.1320440615. Am J Med Genet. 1992. PMID: 1481849
Prenatal recognition of 4p- syndrome.
Blunt S, Berry AC, Seller MJ, Williams CA. Blunt S, et al. Among authors: berry ac. J Med Genet. 1977 Jun;14(3):232-3. doi: 10.1136/jmg.14.3.232. J Med Genet. 1977. PMID: 881719 Free PMC article.
Unknown syndrome: congenital heart disease, choanal stenosis, short stature, developmental delay, and dysmorphic facial features in a brother and sister.
Hurst JA, Berry AC, Tettenborn MA. Hurst JA, et al. Among authors: berry ac. J Med Genet. 1989 Jun;26(6):407-8. doi: 10.1136/jmg.26.6.407. J Med Genet. 1989. PMID: 2472485 Free PMC article.
A new X linked syndrome with mental retardation and craniofacial dysmorphism?
Hyde-Forster I, McCarthy G, Berry AC. Hyde-Forster I, et al. Among authors: berry ac. J Med Genet. 1992 Oct;29(10):736-8. doi: 10.1136/jmg.29.10.736. J Med Genet. 1992. PMID: 1433236 Free PMC article.
A fetus with an X;1 balanced reciprocal translocation and eye disease.
Seller MJ, Pal K, Horsley S, Davies AF, Berry AC, Meredith R, McCartney AC. Seller MJ, et al. Among authors: berry ac. J Med Genet. 1995 Jul;32(7):557-60. doi: 10.1136/jmg.32.7.557. J Med Genet. 1995. PMID: 7562972 Free PMC article.
A child with partial monosomy 6q secondary to a maternal direct insertional event.
Matkins SV, Meyer JE, Berry AC. Matkins SV, et al. Among authors: berry ac. J Med Genet. 1987 Apr;24(4):227-9. doi: 10.1136/jmg.24.4.227. J Med Genet. 1987. PMID: 3585939 Free PMC article.
Two cases of interstitial deletion 1p.
Lai MM, Robards MF, Berry AC, Fear CN, Hart C. Lai MM, et al. Among authors: berry ac. J Med Genet. 1991 Feb;28(2):128-30. doi: 10.1136/jmg.28.2.128. J Med Genet. 1991. PMID: 2002484 Free PMC article.
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