Harvey J - Search Results

1

A reinvestigation of thirty three fragile(X) families using probe StB12.3.

Macpherson J, Harvey J, Curtis G, Webb T, Heitz D, Rousseau F, Jacobs P. Macpherson J, et al. Among authors: harvey j. Am J Med Genet. 1992 Jul 15;43(5):905-12. doi: 10.1002/ajmg.1320430535. Am J Med Genet. 1992. PMID: 1642285

2

Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction.

Fisher JM, Harvey JF, Morton NE, Jacobs PA. Fisher JM, et al. Among authors: harvey jf. Am J Hum Genet. 1995 Mar;56(3):669-75. Am J Hum Genet. 1995. PMID: 7887421 Free PMC article.

3

Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy.

Connarty M, Dennis NR, Patch C, Macpherson JN, Harvey JF. Connarty M, et al. Among authors: harvey jf. Hum Genet. 1996 Jan;97(1):76-8. doi: 10.1007/BF00218837. Hum Genet. 1996. PMID: 8557266

4

A complex rearrangement associated with sex reversal and the Wolf-Hirschhorn syndrome: a cytogenetic and molecular study.

Coles K, Mackenzie M, Crolla J, Harvey J, Starr J, Howard F, Jacobs P. Coles K, et al. Among authors: harvey j. J Med Genet. 1992 Jun;29(6):400-6. doi: 10.1136/jmg.29.6.400. J Med Genet. 1992. PMID: 1619635 Free PMC article.

5

The parental origin of 47,XXY males.

Harvey J, Jacobs PA, Hassold T, Pettay D. Harvey J, et al. Birth Defects Orig Artic Ser. 1990;26(4):289-96. Birth Defects Orig Artic Ser. 1990. PMID: 2090327

6

Molecular studies of trisomy 18.

Fisher JM, Harvey JF, Lindenbaum RH, Boyd PA, Jacobs PA. Fisher JM, et al. Among authors: harvey jf. Am J Hum Genet. 1993 Jun;52(6):1139-44. Am J Hum Genet. 1993. PMID: 8503446 Free PMC article. Review.

7

The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination.

MacDonald M, Hassold T, Harvey J, Wang LH, Morton NE, Jacobs P. MacDonald M, et al. Among authors: harvey j. Hum Mol Genet. 1994 Aug;3(8):1365-71. doi: 10.1093/hmg/3.8.1365. Hum Mol Genet. 1994. PMID: 7987316

8

The origin of sex chromosome aneuploidy.

Jacobs P, Hassold T, Harvey J, May K. Jacobs P, et al. Among authors: harvey j. Prog Clin Biol Res. 1989;311:135-51. Prog Clin Biol Res. 1989. PMID: 2528150 No abstract available.

9

A linkage study of a large pedigree with X linked centronuclear myopathy.

Starr J, Lamont M, Iselius L, Harvey J, Heckmatt J. Starr J, et al. Among authors: harvey j. J Med Genet. 1990 May;27(5):281-3. doi: 10.1136/jmg.27.5.281. J Med Genet. 1990. PMID: 2352255 Free PMC article.

10

A centromere map of the X chromosome from trisomies of maternal origin.

Morton NE, Keats BJ, Jacobs PA, Hassold T, Pettay D, Harvey J, Andrews V. Morton NE, et al. Among authors: harvey j. Ann Hum Genet. 1990 Jan;54(1):39-47. doi: 10.1111/j.1469-1809.1990.tb00359.x. Ann Hum Genet. 1990. PMID: 1969722

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