Lindgren V - Search Results

1

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.

Cook EH Jr, Lindgren V, Leventhal BL, Courchesne R, Lincoln A, Shulman C, Lord C, Courchesne E. Cook EH Jr, et al. Among authors: lindgren v. Am J Hum Genet. 1997 Apr;60(4):928-34. Am J Hum Genet. 1997. PMID: 9106540 Free PMC article.

2

Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.

Lindgren V, Rosinsky B, Chin J, Berry-Kravis E. Lindgren V, et al. Am J Med Genet. 1994 Jan 1;49(1):67-73. doi: 10.1002/ajmg.1320490112. Am J Med Genet. 1994. PMID: 8172253

3

Temple syndrome resulting from uniparental disomy is undiagnosed by a methylation assay due to low-level mosaicism for trisomy 14.

Lindgren V, Cobian K, Bhat G. Lindgren V, et al. Am J Med Genet A. 2021 May;185(5):1538-1543. doi: 10.1002/ajmg.a.62128. Epub 2021 Feb 17. Am J Med Genet A. 2021. PMID: 33595182

4

Do NF1 gene deletions result in a characteristic phenotype?

Tonsgard JH, Yelavarthi KK, Cushner S, Short MP, Lindgren V. Tonsgard JH, et al. Among authors: lindgren v. Am J Med Genet. 1997 Nov 28;73(1):80-6. doi: 10.1002/(sici)1096-8628(19971128)73:1<80::aid-ajmg16>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9375928

5

MLL-SEPT6 fusion transcript with a novel sequence in an infant with acute myeloid leukemia.

Kadkol SS, Bruno A, Oh S, Schmidt ML, Lindgren V. Kadkol SS, et al. Among authors: lindgren v. Cancer Genet Cytogenet. 2006 Jul 15;168(2):162-7. doi: 10.1016/j.cancergencyto.2006.02.020. Cancer Genet Cytogenet. 2006. PMID: 16843108

6

Somatic cell hybrid mapping of human chromosome band 5q31: a region important to hematopoiesis.

Neuman WL, Le Beau MM, Farber RA, Lindgren V, Westbrook CA. Neuman WL, et al. Among authors: lindgren v. Cytogenet Cell Genet. 1992;61(2):103-6. doi: 10.1159/000133381. Cytogenet Cell Genet. 1992. PMID: 1395713

7

Monosomy 22 in two ovarian granulosa cell tumors.

Lindgren V, Waggoner S, Rotmensch J. Lindgren V, et al. Cancer Genet Cytogenet. 1996 Jul 15;89(2):93-7. doi: 10.1016/0165-4608(96)00077-5. Cancer Genet Cytogenet. 1996. PMID: 8697433

8

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes.

Lindgren V, Chen CP, Bryke CR, Lichter P, Page DC, Yang-Feng TL. Lindgren V, et al. Hum Genet. 1992 Feb;88(4):393-8. doi: 10.1007/BF00215672. Hum Genet. 1992. PMID: 1740316

9

Behavioral abnormalities are common and severe in patients with distal 22q11.2 microdeletions and microduplications.

Lindgren V, McRae A, Dineen R, Saulsberry A, Hoganson G, Schrift M. Lindgren V, et al. Mol Genet Genomic Med. 2015 Jul;3(4):346-53. doi: 10.1002/mgg3.146. Epub 2015 Apr 16. Mol Genet Genomic Med. 2015. PMID: 26247050 Free PMC article.

10

Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis.

Lindgren V, Bryke CR, Ozcelik T, Yang-Feng TL, Francke U. Lindgren V, et al. Am J Hum Genet. 1992 May;50(5):988-97. Am J Hum Genet. 1992. PMID: 1315124 Free PMC article. Review.

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