Johnson VP - Search Results

1

Smith-Lemli-Opitz syndrome: review and report of two affected siblings.

Johnson VP. Johnson VP. Z Kinderheilkd. 1975;119(4):221-34. doi: 10.1007/BF00443506. Z Kinderheilkd. 1975. PMID: 166525

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

Correlation of severity and outcome with plasma sterol levels in variants of the Smith-Lemli-Opitz syndrome.

Tint GS, Salen G, Batta AK, Shefer S, Irons M, Elias ER, Abuelo DN, Johnson VP, Lambert M, Lutz R, et al. Tint GS, et al. Among authors: johnson vp. J Pediatr. 1995 Jul;127(1):82-7. doi: 10.1016/s0022-3476(95)70261-x. J Pediatr. 1995. PMID: 7608816

4

The Wolf-Hirschhorn (4p-) syndrome.

Johnson VP, Mulder RD, Hosen R. Johnson VP, et al. Clin Genet. 1976 Aug;10(2NA-NA-760903-760909):104-12. doi: 10.1111/j.1399-0004.1976.tb00021.x. Clin Genet. 1976. PMID: 954225

5

Treatment of Smith-Lemli-Opitz syndrome: results of a multicenter trial.

Irons M, Elias ER, Abuelo D, Bull MJ, Greene CL, Johnson VP, Keppen L, Schanen C, Tint GS, Salen G. Irons M, et al. Among authors: johnson vp. Am J Med Genet. 1997 Jan 31;68(3):311-4. Am J Med Genet. 1997. PMID: 9024565 Clinical Trial.

6

Magnetic resonance imaging of brain anomalies in fetal alcohol syndrome.

Swayze VW 2nd, Johnson VP, Hanson JW, Piven J, Sato Y, Giedd JN, Mosnik D, Andreasen NC. Swayze VW 2nd, et al. Among authors: johnson vp. Pediatrics. 1997 Feb;99(2):232-40. doi: 10.1542/peds.99.2.232. Pediatrics. 1997. PMID: 9024452

7

Martin-Bell syndrome segregating in a large kindred with normal transmitting males: clinical, cytogenetic, and linkage study.

Johnson VP, Carpenter NJ, Skorey PA. Johnson VP, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):275-82. doi: 10.1002/ajmg.1320380222. Am J Med Genet. 1991. PMID: 1673299

8

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

9

A new syndrome of aphalangy, hemivertebrae, and urogenital-intestinal dysgenesis.

Johnson VP, Munson DP. Johnson VP, et al. Clin Genet. 1990 Nov;38(5):346-52. doi: 10.1111/j.1399-0004.1990.tb03593.x. Clin Genet. 1990. PMID: 2282714

10

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.

Papenhausen PR, Mueller OT, Sutcliffe M, Diamond TM, Kousseff BG, Johnson VP. Papenhausen PR, et al. Among authors: johnson vp. Am J Med Genet. 1996 Dec 2;66(1):90. doi: 10.1002/(SICI)1096-8628(19961202)66:1<90::AID-AJMG23>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8957521 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results