Morris MA - Search Results

1

Schizophrenia and chromosomal deletions within 22q11.2.

Lindsay EA, Morris MA, Gos A, Nestadt G, Wolyniec PS, Lasseter VK, Shprintzen R, Antonarakis SE, Baldini A, Pulver AE. Lindsay EA, et al. Among authors: morris ma. Am J Hum Genet. 1995 Jun;56(6):1502-3. Am J Hum Genet. 1995. PMID: 7762575 Free PMC article. No abstract available.

2

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

Karayiorgou M, Morris MA, Morrow B, Shprintzen RJ, Goldberg R, Borrow J, Gos A, Nestadt G, Wolyniec PS, Lasseter VK, et al. Karayiorgou M, et al. Among authors: morris ma. Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7612-6. doi: 10.1073/pnas.92.17.7612. Proc Natl Acad Sci U S A. 1995. PMID: 7644464 Free PMC article.

3

A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.

Blouin JL, Christie DH, Gos A, Lynn A, Morris MA, Ledbetter DH, Chakravarti A, Antonarakis SE. Blouin JL, et al. Among authors: morris ma. Am J Hum Genet. 1995 Aug;57(2):388-94. Am J Hum Genet. 1995. PMID: 7668265 Free PMC article.

4

A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region.

Bartsch O, Hinkel GK, Petersen MB, König U, Bugge M, Mikkelsen M, Avramopoulos D, Morris M, Antonarakis SE. Bartsch O, et al. Hum Genet. 1997 Oct;100(5-6):669-75. doi: 10.1007/s004390050571. Hum Genet. 1997. PMID: 9341890

5

Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13.

Eliez S, Morris MA, Dahoun-Hadorn S, DeLozier-Blanchet CD, Gos A, Sizonenko P, Antonarakis SE. Eliez S, et al. Among authors: morris ma. Am J Med Genet. 1997 Jun 13;70(3):222-8. doi: 10.1002/(sici)1096-8628(19970613)70:3<222::aid-ajmg3>3.0.co;2-y. Am J Med Genet. 1997. PMID: 9188657

6

A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y.

Chen H, Rossier C, Morris MA, Scott HS, Gos A, Bairoch A, Antonarakis SE. Chen H, et al. Among authors: morris ma. Hum Genet. 1999 Nov;105(5):399-409. doi: 10.1007/s004390051122. Hum Genet. 1999. PMID: 10598804

7

Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study.

Eliez S, Antonarakis SE, Morris MA, Dahoun SP, Reiss AL. Eliez S, et al. Among authors: morris ma. Arch Gen Psychiatry. 2001 Jan;58(1):64-8. doi: 10.1001/archpsyc.58.1.64. Arch Gen Psychiatry. 2001. PMID: 11146759

8

Exon skipping associated with A-->G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene.

Hutter P, Antonarakis SE, Delozier-Blanchet CD, Morris MA. Hutter P, et al. Among authors: morris ma. Hum Mol Genet. 1994 Apr;3(4):663-5. doi: 10.1093/hmg/3.4.663. Hum Mol Genet. 1994. PMID: 8069315 No abstract available.

9

Dinucleotide repeat polymorphism within ERCC5 gene.

Samec S, Clarkson SG, Blaschak J, Chakravarti A, Morris MA, Scherly D, Antonarakis SE. Samec S, et al. Among authors: morris ma. Hum Mol Genet. 1994 Jan;3(1):214. doi: 10.1093/hmg/3.1.214-a. Hum Mol Genet. 1994. PMID: 8162040 No abstract available.

10

Fortuitous detection of uniparental isodisomy of chromosome 6.

Bittencourt MC, Morris MA, Chabod J, Gos A, Lamy B, Fellmann F, Antonarakis SE, Plouvier E, Herve P, Tiberghien P. Bittencourt MC, et al. Among authors: morris ma. J Med Genet. 1997 Jan;34(1):77-8. doi: 10.1136/jmg.34.1.77. J Med Genet. 1997. PMID: 9032654 Free PMC article.

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