Hoehn H - Search Results

1

Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome.

Gong BT, Norwood TH, Hoehn H, McPherson E, Hall JG, Hickman R. Gong BT, et al. Among authors: hoehn h. Hum Genet. 1976 Dec 29;35(1):117-23. doi: 10.1007/BF00295627. Hum Genet. 1976. PMID: 1002161

2

Small structural changes of chromosome 8. Two cases with evidence for deletion.

Beighle C, Karp LE, Hanson JW, Hall JG, Hoehn H. Beighle C, et al. Among authors: hoehn h. Hum Genet. 1977 Aug 31;38(1):113-21. doi: 10.1007/BF00295814. Hum Genet. 1977. PMID: 903151

3

Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes.

Pagon RA, Hall JG, Davenport SL, Aase J, Norwood TH, Hoehn HW. Pagon RA, et al. Among authors: hoehn hw. Am J Hum Genet. 1979 Jan;31(1):54-61. Am J Hum Genet. 1979. PMID: 155399 Free PMC article.

4

Trisomy of the long arm of human chromosome 1.

Norwood TH, Hoehn H. Norwood TH, et al. Among authors: hoehn h. Humangenetik. 1974;25(1):79-82. doi: 10.1007/BF00281010. Humangenetik. 1974. PMID: 4442882 No abstract available.

5

Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

Jennings M, Hall JG, Hoehn H. Jennings M, et al. Among authors: hoehn h. Am J Med Genet. 1980;7(4):417-32. doi: 10.1002/ajmg.1320070404. Am J Med Genet. 1980. PMID: 6938131

6

Mosaicism in amniotic fluid cell cultures: classification and significance.

Hoehn H, Rodriguez ML, Norwood TH, Maxwell CL. Hoehn H, et al. Am J Med Genet. 1978;2(3):253-66. doi: 10.1002/ajmg.1320020306. Am J Med Genet. 1978. PMID: 400764 Review.

7

Amniotic fluid cell mosaicism for presumptive trisomy 20.

Rodriguez ML, Luthy D, Hall JG, Norwood TH, Hoehn H. Rodriguez ML, et al. Among authors: hoehn h. Clin Genet. 1978 Feb;13(2):164-8. doi: 10.1111/j.1399-0004.1978.tb04245.x. Clin Genet. 1978. PMID: 637912

8

Variegated translocation mosaicism in human skin fibroblast cultures.

Hoehn H, Bryant EM, Au K, Norwood TH, Boman H, Martin GM. Hoehn H, et al. Cytogenet Cell Genet. 1975;15(5):282-98. doi: 10.1159/000130526. Cytogenet Cell Genet. 1975. PMID: 1222585

9

No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45, XO Turner syndrome.

Burns JL, Hall JG, Powers E, Callis JB, Hoehn H. Burns JL, et al. Among authors: hoehn h. Clin Genet. 1979 Jan;15(1):22-8. doi: 10.1111/j.1399-0004.1979.tb02025.x. Clin Genet. 1979. PMID: 759054

10

Prenatal genetic diagnosis and elective abortion in women over 35: utilization and relative impact on the birth prevalence of Down syndrome in Washington State.

Luthy DA, Emanuel I, Hoehn H, Hall JG, Powers EK. Luthy DA, et al. Among authors: hoehn h. Am J Med Genet. 1980;7(3):375-81. doi: 10.1002/ajmg.1320070320. Am J Med Genet. 1980. PMID: 6451173

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