Hofman KJ - Search Results

1

Smith-Lemli-Opitz syndrome: prenatal diagnosis by quantification of cholesterol precursors in amniotic fluid.

Rossiter JP, Hofman KJ, Kelley RI. Rossiter JP, et al. Among authors: hofman kj. Am J Med Genet. 1995 Apr 10;56(3):272-5. doi: 10.1002/ajmg.1320560307. Am J Med Genet. 1995. PMID: 7778588

2

Attitudes of physicians and genetics professionals toward cystic fibrosis carrier screening.

Faden RR, Tambor ES, Chase GA, Geller G, Hofman KJ, Holtzman NA. Faden RR, et al. Among authors: hofman kj. Am J Med Genet. 1994 Mar 1;50(1):1-11. doi: 10.1002/ajmg.1320500102. Am J Med Genet. 1994. PMID: 8160745

3

Physicians' knowledge of genetics and genetic tests.

Hofman KJ, Tambor ES, Chase GA, Geller G, Faden RR, Holtzman NA. Hofman KJ, et al. Acad Med. 1993 Aug;68(8):625-32. doi: 10.1097/00001888-199308000-00013. Acad Med. 1993. PMID: 8352875

4

Marfan syndrome: neuropsychological aspects.

Hofman KJ, Bernhardt BA, Pyeritz RE. Hofman KJ, et al. Am J Med Genet. 1988 Oct;31(2):331-8. doi: 10.1002/ajmg.1320310210. Am J Med Genet. 1988. PMID: 3232699

5

Diffusion of information about neurofibromatosis type 1 DNA testing.

Hofman KJ. Hofman KJ. Am J Med Genet. 1994 Feb 1;49(3):299-301. doi: 10.1002/ajmg.1320490311. Am J Med Genet. 1994. PMID: 8209889

6

Offering cystic fibrosis carrier screening to an HMO population: factors associated with utilization.

Tambor ES, Bernhardt BA, Chase GA, Faden RR, Geller G, Hofman KJ, Holtzman NA. Tambor ES, et al. Among authors: hofman kj. Am J Hum Genet. 1994 Oct;55(4):626-37. Am J Hum Genet. 1994. PMID: 7942840 Free PMC article.

7

Phenylketonuria in U.S. blacks: molecular analysis of the phenylalanine hydroxylase gene.

Hofman KJ, Steel G, Kazazian HH, Valle D. Hofman KJ, et al. Am J Hum Genet. 1991 Apr;48(4):791-8. Am J Hum Genet. 1991. PMID: 2014802 Free PMC article.

8

Familial neurofibromatosis type 1: clinical experience with DNA testing.

Hofman KJ, Boehm CD. Hofman KJ, et al. J Pediatr. 1992 Mar;120(3):394-8. doi: 10.1016/s0022-3476(05)80903-5. J Pediatr. 1992. PMID: 1347082

9

Familial systematized epidermal nevus syndrome.

Meschia JF, Junkins E, Hofman KJ. Meschia JF, et al. Among authors: hofman kj. Am J Med Genet. 1992 Nov 15;44(5):664-7. doi: 10.1002/ajmg.1320440527. Am J Med Genet. 1992. PMID: 1481830 Review.

10

Relationship between T2-weighted hyperintensities (unidentified bright objects) and lower IQs in children with neurofibromatosis-1.

Denckla MB, Hofman K, Mazzocco MM, Melhem E, Reiss AL, Bryan RN, Harris EL, Lee J, Cox CS, Schuerholz LJ. Denckla MB, et al. Am J Med Genet. 1996 Feb 16;67(1):98-102. doi: 10.1002/(SICI)1096-8628(19960216)67:1<98::AID-AJMG17>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8678124

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