Kasch LM - Search Results

1

A paternally derived inverted duplication of 7q with evidence of a telomeric deletion.

Stetten G, Charity LL, Kasch LM, Scott AF, Berman CL, Pressman E, Blakemore KJ. Stetten G, et al. Among authors: kasch lm. Am J Med Genet. 1997 Jan 10;68(1):76-81. Am J Med Genet. 1997. PMID: 8986281

2

The use of polymerase chain reaction to determine fetal RhD status.

Rossiter JP, Blakemore KJ, Kickler TS, Kasch LM, Khouzami AN, Pressman EK, Sciscione AC, Kazazian HH Jr. Rossiter JP, et al. Among authors: kasch lm. Am J Obstet Gynecol. 1994 Oct;171(4):1047-51. doi: 10.1016/0002-9378(94)90032-9. Am J Obstet Gynecol. 1994. PMID: 7943068 Clinical Trial.

3

Schizophrenia: a genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes.

Pulver AE, Lasseter VK, Kasch L, Wolyniec P, Nestadt G, Blouin JL, Kimberland M, Babb R, Vourlis S, Chen H, et al. Pulver AE, et al. Am J Med Genet. 1995 Jun 19;60(3):252-60. doi: 10.1002/ajmg.1320600316. Am J Med Genet. 1995. PMID: 7573181

4

Genetic and environmental risk factors for sagittal craniosynostosis.

Zeiger JS, Beaty TH, Hetmanski JB, Wang H, Scott AF, Kasch L, Raymond G, Jabs EW, VanderKolk C. Zeiger JS, et al. J Craniofac Surg. 2002 Sep;13(5):602-6. doi: 10.1097/00001665-200209000-00002. J Craniofac Surg. 2002. PMID: 12218784

5

Identification of an HMGB3 frameshift mutation in a family with an X-linked colobomatous microphthalmia syndrome using whole-genome and X-exome sequencing.

Scott AF, Mohr DW, Kasch LM, Barton JA, Pittiglio R, Ingersoll R, Craig B, Marosy BA, Doheny KF, Bromley WC, Roderick TH, Chassaing N, Calvas P, Prabhu SS, Jabs EW. Scott AF, et al. Among authors: kasch lm. JAMA Ophthalmol. 2014 Oct;132(10):1215-20. doi: 10.1001/jamaophthalmol.2014.1731. JAMA Ophthalmol. 2014. PMID: 24993872

6

Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2.

Pulver AE, Karayiorgou M, Lasseter VK, Wolyniec P, Kasch L, Antonarakis S, Housman D, Kazazian HH, Meyers D, Nestadt G, et al. Pulver AE, et al. Am J Med Genet. 1994 Mar 15;54(1):44-50. doi: 10.1002/ajmg.1320540109. Am J Med Genet. 1994. PMID: 7909990

7

Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1.

Pulver AE, Karayiorgou M, Wolyniec PS, Lasseter VK, Kasch L, Nestadt G, Antonarakis S, Housman D, Kazazian HH, Meyers D, et al. Pulver AE, et al. Am J Med Genet. 1994 Mar 15;54(1):36-43. doi: 10.1002/ajmg.1320540108. Am J Med Genet. 1994. PMID: 8178837

8

Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations of the cystic fibrosis gene.

Cutting GR, Antonarakis SE, Buetow KH, Kasch LM, Rosenstein BJ, Kazazian HH Jr. Cutting GR, et al. Among authors: kasch lm. Am J Hum Genet. 1989 Mar;44(3):307-18. Am J Hum Genet. 1989. PMID: 2563631 Free PMC article.

9

Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3.

Lasseter VK, Pulver AE, Wolyniec PS, Nestadt G, Meyers D, Karayiorgou M, Housman D, Antonarakis S, Kazazian H, Kasch L, et al. Lasseter VK, et al. Am J Med Genet. 1995 Apr 24;60(2):172-3. doi: 10.1002/ajmg.1320600217. Am J Med Genet. 1995. PMID: 7485255 No abstract available.

10

Physical map of the chromosome 6q22 region containing the oculodentodigital dysplasia locus: analysis of thirteen candidate genes and identification of novel ESTs and DNA polymorphisms.

Boyadjiev SA, Chowdry AB, Shapiro RE, Paznekas WA, Wandstrat AE, Choi JW, Kasch L, Zhang G, Wollnik B, Burgess CE, Schalling M, Lovett M, Jabs EW. Boyadjiev SA, et al. Cytogenet Genome Res. 2002;98(1):29-37. doi: 10.1159/000068535. Cytogenet Genome Res. 2002. PMID: 12584438

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