Levin SW - Search Results

1

DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndrome.

Correa-Cerro LS, Wassif CA, Waye JS, Krakowiak PA, Cozma D, Dobson NR, Levin SW, Anadiotis G, Steiner RD, Krajewska-Walasek M, Nowaczyk MJ, Porter FD. Correa-Cerro LS, et al. Among authors: levin sw. J Med Genet. 2005 Apr;42(4):350-7. doi: 10.1136/jmg.2004.022749. J Med Genet. 2005. PMID: 15805162 Free PMC article. No abstract available.

2

Unusual renal features of Lowe syndrome in a mildly affected boy.

Gropman A, Levin S, Yao L, Lin T, Suchy S, Sabnis S, Hadley D, Nussbaum R. Gropman A, et al. Am J Med Genet. 2000 Dec 18;95(5):461-6. doi: 10.1002/1096-8628(20001218)95:5<461::aid-ajmg10>3.0.co;2-d. Am J Med Genet. 2000. PMID: 11146467

3

Molecularly defined interstitial tandem duplication 6p case with mild manifestations.

Ng D, Mowrey P, Ragoussis J, Mirza G, Coll E, Di Fazio MP, Turner C, Levin SW. Ng D, et al. Among authors: levin sw. Am J Med Genet. 2001 Nov 1;103(4):320-5. Am J Med Genet. 2001. PMID: 11746013

4

1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child.

Cobb W, Anderson A, Turner C, Hoffman RD, Schonberg S, Levin SW. Cobb W, et al. Among authors: levin sw. Eur J Med Genet. 2010 Nov-Dec;53(6):415-8. doi: 10.1016/j.ejmg.2010.08.009. Epub 2010 Sep 9. Eur J Med Genet. 2010. PMID: 20832509

5

Isolated bilateral anophthalmia in a girl with an apparently balanced de novo translocation: 46,XX,t(3;11)(q27;p11.2).

Driggers RW, Macri CJ, Greenwald J, Carpenter D, Avallone J, Howard-Peebles PN, Levin SW. Driggers RW, et al. Among authors: levin sw. Am J Med Genet. 1999 Nov 26;87(3):201-2. doi: 10.1002/(sici)1096-8628(19991126)87:3<201::aid-ajmg1>3.0.co;2-h. Am J Med Genet. 1999. PMID: 10564870 Review.

6

Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin.

Lacbawan FL, White BJ, Anguiano A, Rigdon DT, Ball KD, Bromage GB, Yang X, DiFazio MP, Levin SW. Lacbawan FL, et al. Among authors: levin sw. Am J Med Genet. 1999 Nov 19;87(2):139-42. Am J Med Genet. 1999. PMID: 10533028 Review.

7

Acrofacial dysostosis with ambiguous genitalia.

Wulfsberg EA, Curtis J, Wiswell TE, Puntel RA, Levin SW. Wulfsberg EA, et al. Among authors: levin sw. Am J Med Genet. 1990 Nov;37(3):384-7. doi: 10.1002/ajmg.1320370318. Am J Med Genet. 1990. PMID: 2260569

8

Balanced rearrangement of chromosomes 2, 5, and 13 in a family with duplication 5q and fetal loss.

Evans MI, White BJ, Kent SG, Levine MA, Levin SW, Larsen JW Jr. Evans MI, et al. Among authors: levin sw. Am J Med Genet. 1984 Dec;19(4):783-90. doi: 10.1002/ajmg.1320190419. Am J Med Genet. 1984. PMID: 6517101

9

MRI Brain Volume Measurements in Infantile Neuronal Ceroid Lipofuscinosis.

Baker EH, Levin SW, Zhang Z, Mukherjee AB. Baker EH, et al. Among authors: levin sw. AJNR Am J Neuroradiol. 2017 Feb;38(2):376-382. doi: 10.3174/ajnr.A4978. Epub 2016 Oct 20. AJNR Am J Neuroradiol. 2017. PMID: 27765741 Free PMC article.

10

Evaluation of disease progression in INCL by MR spectroscopy.

Baker EH, Levin SW, Zhang Z, Mukherjee AB. Baker EH, et al. Among authors: levin sw. Ann Clin Transl Neurol. 2015 Aug;2(8):797-809. doi: 10.1002/acn3.222. Epub 2015 Jul 1. Ann Clin Transl Neurol. 2015. PMID: 26339674 Free PMC article.

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

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

27 results

Search Page

Filters