Hall JG - Search Results

1

Cohen T, Zeitune M, McGillivray BC, Hall JG, Lynn AH, Aston CE, Chakravarti A. Cohen T, et al. Among authors: hall jg. Am J Med Genet. 1996 Oct 28;65(3):226-34. doi: 10.1002/(SICI)1096-8628(19961028)65:3<226::AID-AJMG11>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 9240749

2

Bleeding diathesis in Noonan syndrome: a common association.

Witt DR, McGillivray BC, Allanson JE, Hughes HE, Hathaway WE, Zipursky A, Hall JG. Witt DR, et al. Among authors: hall jg. Am J Med Genet. 1988 Oct;31(2):305-17. doi: 10.1002/ajmg.1320310208. Am J Med Genet. 1988. PMID: 3232698

3

Familial renal hypophosphatemia, minor facial anomalies, intracerebral calcifications, and non-rachitic bone changes: apparently new syndrome?

Chitayat D, McGillivray BC, Rothstein R, Flodmark O, Priddy RW, Ebelt VJ, Lirenman DS, Hall JG. Chitayat D, et al. Among authors: hall jg. Am J Med Genet. 1990 Mar;35(3):406-14. doi: 10.1002/ajmg.1320350318. Am J Med Genet. 1990. PMID: 2309790

4

Part II. Amyoplasia: twinning in amyoplasia--a specific type of arthrogryposis with an apparent excess of discordantly affected identical twins.

Hall JG, Reed SD, McGillivray BC, Herrmann J, Partington MW, Schinzel A, Shapiro J, Weaver DD. Hall JG, et al. Am J Med Genet. 1983 Aug;15(4):591-9. doi: 10.1002/ajmg.1320150408. Am J Med Genet. 1983. PMID: 6684397

5

Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feet.

Chitayat D, Davis EB, McGillivray BC, Hayden MR, Hall JG. Chitayat D, et al. Among authors: hall jg. Clin Genet. 1989 Mar;35(3):161-6. doi: 10.1111/j.1399-0004.1989.tb02923.x. Clin Genet. 1989. PMID: 2706799

6

Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).

Froster-Iskenius U, McGillivray BC, Dill FJ, Hall JG, Herbst DS. Froster-Iskenius U, et al. Among authors: hall jg. Am J Med Genet. 1986 Jan-Feb;23(1-2):619-31. doi: 10.1002/ajmg.1320230156. Am J Med Genet. 1986. PMID: 3953672

7

Tuberous sclerosis: case report and investigation of family members.

Wilson RD, Hall JG, McGillivray BC. Wilson RD, et al. Among authors: hall jg. Can Med Assoc J. 1985 Apr 1;132(7):807-9. Can Med Assoc J. 1985. PMID: 3978502 Free PMC article.

8

Molecular nosology of heritable disorders of connective tissue.

Beighton P, De Paepe A, Hall JG, Hollister DW, Pope FM, Pyeritz RE, Steinmann B, Tsipouras P. Beighton P, et al. Among authors: hall jg. Am J Med Genet. 1992 Feb 15;42(4):431-48. doi: 10.1002/ajmg.1320420406. Am J Med Genet. 1992. PMID: 1609825 No abstract available.

9

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.

Rajcan-Separovic E, Harvard C, Liu X, McGillivray B, Hall JG, Qiao Y, Hurlburt J, Hildebrand J, Mickelson EC, Holden JJ, Lewis ME. Rajcan-Separovic E, et al. Among authors: hall jg. J Med Genet. 2007 Apr;44(4):269-76. doi: 10.1136/jmg.2006.045013. Epub 2006 Sep 8. J Med Genet. 2007. PMID: 16963482 Free PMC article.

10

Nonimmune hydrops fetalis.

McGillivray BC, Hall JG. McGillivray BC, et al. Among authors: hall jg. Pediatr Rev. 1987 Dec;9(6):197-202. doi: 10.1542/pir.9-6-197. Pediatr Rev. 1987. PMID: 3332376 Review. No abstract available.

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