Kasch LM - Search Results

1

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.

2

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

3

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

4

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein.

Cutting GR, Kasch LM, Rosenstein BJ, Zielenski J, Tsui LC, Antonarakis SE, Kazazian HH Jr. Cutting GR, et al. Among authors: kasch lm. Nature. 1990 Jul 26;346(6282):366-9. doi: 10.1038/346366a0. Nature. 1990. PMID: 1695717

5

Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region on human chromosome 2.

Cutting GR, McGinniss MJ, Kasch LM, Tsipouras P, Antonarakis SE. Cutting GR, et al. Among authors: kasch lm. Genomics. 1990 Oct;8(2):407-10. doi: 10.1016/0888-7543(90)90302-b. Genomics. 1990. PMID: 1979060 Free article.

6

Two patients with cystic fibrosis, nonsense mutations in each cystic fibrosis gene, and mild pulmonary disease.

Cutting GR, Kasch LM, Rosenstein BJ, Tsui LC, Kazazian HH Jr, Antonarakis SE. Cutting GR, et al. Among authors: kasch lm. N Engl J Med. 1990 Dec 13;323(24):1685-9. doi: 10.1056/NEJM199012133232407. N Engl J Med. 1990. PMID: 2233965 Free article. No abstract available.

7

Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene.

Higuchi M, Kazazian HH Jr, Kasch L, Warren TC, McGinniss MJ, Phillips JA 3rd, Kasper C, Janco R, Antonarakis SE. Higuchi M, et al. Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):7405-9. doi: 10.1073/pnas.88.16.7405. Proc Natl Acad Sci U S A. 1991. PMID: 1908096 Free PMC article.

8

Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis.

Higuchi M, Antonarakis SE, Kasch L, Oldenburg J, Economou-Petersen E, Olek K, Arai M, Inaba H, Kazazian HH Jr. Higuchi M, et al. Proc Natl Acad Sci U S A. 1991 Oct 1;88(19):8307-11. doi: 10.1073/pnas.88.19.8307. Proc Natl Acad Sci U S A. 1991. PMID: 1924291 Free PMC article.

9

Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's disease.

Brandt J, Quaid KA, Folstein SE, Garber P, Maestri NE, Abbott MH, Slavney PR, Franz ML, Kasch L, Kazazian HH Jr. Brandt J, et al. JAMA. 1989 Jun 2;261(21):3108-14. JAMA. 1989. PMID: 2523979

10

Prenatal testing for Huntington disease.

Corson V, Quaid K, Kasch L, Kazazian HH Jr. Corson V, et al. Birth Defects Orig Artic Ser. 1990;26(3):226-30. Birth Defects Orig Artic Ser. 1990. PMID: 2151181 No abstract available.

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