Hall JG - Search Results

1

Wilson RD, Traverse L, Hall JG, Flodmark CO, Rootman J. Wilson RD, et al. Among authors: hall jg. Am J Ophthalmol. 1985 Feb 15;99(2):142-8. doi: 10.1016/0002-9394(85)90222-3. Am J Ophthalmol. 1985. PMID: 3970117

2

De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.

Chitayat D, Fagerstrom CL, Kalousek DK, Rootman J, Taylor GP, Hall JG. Chitayat D, et al. Among authors: hall jg. Am J Med Genet. 1989 Jan;32(1):36-41. doi: 10.1002/ajmg.1320320109. Am J Med Genet. 1989. PMID: 2495721

3

Familial multiple exostoses--no chromosome 8 deletion observed.

Hall JG, Wilson RD, Kalousek D, Beauchamp R. Hall JG, et al. Am J Med Genet. 1985 Nov;22(3):639-40. doi: 10.1002/ajmg.1320220328. Am J Med Genet. 1985. PMID: 4061499 No abstract available.

4

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.

5

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.

Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG. Bamforth JS, et al. Among authors: hall jg. Am J Med Genet. 1989 Jan;32(1):93-9. doi: 10.1002/ajmg.1320320120. Am J Med Genet. 1989. PMID: 2650550

6

Three-generation dominant transmission of the Silver-Russell syndrome.

Duncan PA, Hall JG, Shapiro LR, Vibert BK. Duncan PA, et al. Among authors: hall jg. Am J Med Genet. 1990 Feb;35(2):245-50. doi: 10.1002/ajmg.1320350220. Am J Med Genet. 1990. PMID: 2178417 Review.

7

Comments on the Neu-Laxova syndrome and CAD complex.

Scott CI, Louro JM, Laurence KM, Tolarová M, Hall JG, Reed S, Curry CJ. Scott CI, et al. Among authors: hall jg. Am J Med Genet. 1981;9(2):165-75. doi: 10.1002/ajmg.1320090211. Am J Med Genet. 1981. PMID: 7258229 No abstract available.

8

Part I. Amyoplasia: a common, sporadic condition with congenital contractures.

Hall JG, Reed SD, Driscoll EP. Hall JG, et al. Am J Med Genet. 1983 Aug;15(4):571-90. doi: 10.1002/ajmg.1320150407. Am J Med Genet. 1983. PMID: 6614047

9

Brief clinical report: an unusual bandlike web in an infant with lethal multiple pterygium syndrome.

Froster-Iskenius UG, Curry C, Philp M, Hall JG. Froster-Iskenius UG, et al. Among authors: hall jg. Am J Med Genet. 1988 Jul;30(3):763-9. doi: 10.1002/ajmg.1320300310. Am J Med Genet. 1988. PMID: 3189397

10

Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly--a new syndrome? Part II: Neuropathological considerations.

Clarren SK, Alvord EC Jr, Hall JG. Clarren SK, et al. Among authors: hall jg. Am J Med Genet. 1980;7(1):75-83. doi: 10.1002/ajmg.1320070111. Am J Med Genet. 1980. PMID: 7211954

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