Dasouki MJ - Search Results

1

Heterogeneity in hereditary pancreatitis.

Dasouki MJ, Cogan J, Summar ML, Neblitt W 3rd, Foroud T, Koller D, Phillips JA 3rd. Dasouki MJ, et al. Am J Med Genet. 1998 Apr 28;77(1):47-53. Am J Med Genet. 1998. PMID: 9557894

2

DiGeorge anomaly and chromosome 10p deletions: one or two loci?

Dasouki M, Jurecic V, Phillips JA 3rd, Whitlock JA, Baldini A. Dasouki M, et al. Am J Med Genet. 1997 Nov 28;73(1):72-5. Am J Med Genet. 1997. PMID: 9375926

3

Assignment of the gene (GLCLC) that encodes the heavy subunit of gamma-glutamylcysteine synthetase to human chromosome 6.

Sierra-Rivera E, Summar ML, Dasouki M, Krishnamani MR, Phillips JA, Freeman ML. Sierra-Rivera E, et al. Cytogenet Cell Genet. 1995;70(3-4):278-9. doi: 10.1159/000134051. Cytogenet Cell Genet. 1995. PMID: 7789189

4

Assignment of the human gene (GLCLR) that encodes the regulatory subunit of gamma-glutamylcysteine synthetase to chromosome 1p21.

Sierra-Rivera E, Dasouki M, Summar ML, Krishnamani MR, Meredith M, Rao PN, Phillips JA 3rd, Freeman ML. Sierra-Rivera E, et al. Cytogenet Cell Genet. 1996;72(2-3):252-4. doi: 10.1159/000134202. Cytogenet Cell Genet. 1996. PMID: 8978789

5

Physical and linkage mapping of human carbamyl phosphate synthetase I (CPS1) and reassignment from 2p to 2q35.

Summar ML, Dasouki MJ, Schofield PJ, Krishnamani MR, Vnencak-Jones C, Tuchman M, Mao J, Phillips JA 3rd. Summar ML, et al. Among authors: dasouki mj. Cytogenet Cell Genet. 1995;71(3):266-7. doi: 10.1159/000134124. Cytogenet Cell Genet. 1995. PMID: 7587391

6

Human selenoprotein P gene maps to 5q31.

Hill KE, Dasouki M, Phillips JA 3rd, Burk RF. Hill KE, et al. Genomics. 1996 Sep 15;36(3):550-1. doi: 10.1006/geno.1996.0505. Genomics. 1996. PMID: 8884283 No abstract available.

7

Use of a probe for the putative sex determining gene, zinc finger Y, in the study of patients with ambiguous genitalia and XY gonadal dysgenesis.

Erickson RP, Verga V, Dasouki M. Erickson RP, et al. Am J Med Genet. 1990 Jun;36(2):232-6. doi: 10.1002/ajmg.1320360218. Am J Med Genet. 1990. PMID: 2368811 Free article.

8

Childhood hyperuricemia and acute renal failure resulting from a missense mutation in the HPRT gene.

Srivastava T, O'Neill JP, Dasouki M, Simckes AM. Srivastava T, et al. Am J Med Genet. 2002 Mar 15;108(3):219-22. doi: 10.1002/ajmg.10217. Am J Med Genet. 2002. PMID: 11891689

9

Translocation (1;22) in a child with bilateral oblique facial clefts.

Dasouki M, Barr M Jr, Erickson RP, Cox B. Dasouki M, et al. J Med Genet. 1988 Jun;25(6):427-9. doi: 10.1136/jmg.25.6.427. J Med Genet. 1988. PMID: 3398011 Free PMC article.

10

The 3q29 microdeletion syndrome: report of three new unrelated patients and in silico "RNA binding" analysis of the 3q29 region.

Dasouki MJ, Lushington GH, Hovanes K, Casey J, Gorre M. Dasouki MJ, et al. Am J Med Genet A. 2011 Jul;155A(7):1654-60. doi: 10.1002/ajmg.a.34080. Epub 2011 May 27. Am J Med Genet A. 2011. PMID: 21626679 Free PMC article.

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