Johnson VP - Search Results

1

Natural history of mosaic trisomy 14 syndrome.

Fujimoto A, Allanson J, Crowe CA, Lipson MH, Johnson VP. Fujimoto A, et al. Among authors: johnson vp. Am J Med Genet. 1992 Sep 15;44(2):189-96. doi: 10.1002/ajmg.1320440214. Am J Med Genet. 1992. PMID: 1456290 Review.

2

Trisomy 14 mosaicism: case report and review.

Johnson VP, Aceto T Jr, Likness C. Johnson VP, et al. Am J Med Genet. 1979;3(4):331-9. doi: 10.1002/ajmg.1320030404. Am J Med Genet. 1979. PMID: 474633

3

Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs.

Altherr MR, Wright TJ, Denison K, Perez-Castro AV, Johnson VP. Altherr MR, et al. Among authors: johnson vp. Am J Med Genet. 1997 Jul 11;71(1):47-53. doi: 10.1002/(sici)1096-8628(19970711)71:1<47::aid-ajmg9>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9215768

4

Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndrome.

Altherr MR, Gusella JF, Wasmuth JJ, Kummer MA, McKercher SW, Johnson VP. Altherr MR, et al. Among authors: johnson vp. Am J Med Genet. 1992 Nov 1;44(4):449-54. doi: 10.1002/ajmg.1320440413. Am J Med Genet. 1992. PMID: 1442886

5

Deletion of the distal long arm of chromosome 1: a definable syndrome.

Johnson VP, Heck LJ, Carter GA, Flom JO. Johnson VP, et al. Am J Med Genet. 1985 Dec;22(4):685-94. doi: 10.1002/ajmg.1320220405. Am J Med Genet. 1985. PMID: 4073121

6

Fetal alcohol syndrome: craniofacial and central nervous system manifestations.

Johnson VP, Swayze VW II, Sato Y, Andreasen NC. Johnson VP, et al. Am J Med Genet. 1996 Feb 2;61(4):329-39. doi: 10.1002/(SICI)1096-8628(19960202)61:4<329::AID-AJMG6>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8834044

7

A new case of Grange syndrome without cardiac findings.

Wallerstein R, Augustyn AM, Wallerstein D, Elton L, Tejeiro B, Johnson V, Lieberman K. Wallerstein R, et al. Am J Med Genet A. 2006 Jun 15;140(12):1316-20. doi: 10.1002/ajmg.a.31125. Am J Med Genet A. 2006. PMID: 16691574

8

FISH detection of Wolf-Hirschhorn syndrome: exclusion of D4F26 as critical site.

Johnson VP, Altherr MR, Blake JM, Keppen LD. Johnson VP, et al. Am J Med Genet. 1994 Aug 1;52(1):70-4. doi: 10.1002/ajmg.1320520114. Am J Med Genet. 1994. PMID: 7977466

9

A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism.

Johnson VP, McMillin JM, Aceto T Jr, Bruins G. Johnson VP, et al. Am J Med Genet. 1983 Jul;15(3):497-506. doi: 10.1002/ajmg.1320150316. Am J Med Genet. 1983. PMID: 6881216

10

Duplication of the distal part of the long arm of chromosome 1.

Johnson VP. Johnson VP. Am J Med Genet. 1991 Jun 1;39(3):258-69. doi: 10.1002/ajmg.1320390305. Am J Med Genet. 1991. PMID: 1867275 Review.

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