Rao N - Search Results

1

Physical and cDNA mapping in the DBH region of human chromosome 9q34.

Gilbert JR, Kumar A, Newey S, Rao N, Ioannou P, Qiu H, Lin D, Xu P, Pettenati MJ, Pericak-Vance MA. Gilbert JR, et al. Among authors: rao n. Hum Hered. 2000 May-Jun;50(3):151-7. doi: 10.1159/000022905. Hum Hered. 2000. PMID: 10686491

2

Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.

Othmane KB, Loeb D, Hayworth-Hodgte R, Hentati F, Rao N, Roses AD, Ben Hamida M, Pericak-Vance MA, Vance JM. Othmane KB, et al. Among authors: rao n. Genomics. 1995 Jul 20;28(2):286-90. doi: 10.1006/geno.1995.1143. Genomics. 1995. PMID: 8530038

3

Fine localization of the CMT4A locus using a PAC contig and haplotype analysis.

Ben Othmane K, Rochelle JM, Ben Hamida M, Slotterbeck B, Rao N, Hentati F, Pericak-Vance MA, Vance JM. Ben Othmane K, et al. Among authors: rao n. Neurogenetics. 1998 Dec;2(1):18-23. doi: 10.1007/s100480050047. Neurogenetics. 1998. PMID: 9933296

4

Triple trisomy in a 17-week-old fetus.

Pettenati MJ, Rao N. Pettenati MJ, et al. Among authors: rao n. Hum Genet. 1991 Jun;87(2):239-40. doi: 10.1007/BF00204194. Hum Genet. 1991. PMID: 2066117

5

Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation.

Pettenati MJ, Rao N, Johnson C, Hayworth R, Crandall K, Huff O, Thomas IT. Pettenati MJ, et al. Among authors: rao n. Hum Genet. 1992 Aug;89(6):602-6. doi: 10.1007/BF00221946. Hum Genet. 1992. PMID: 1511976 Review.

6

De novo inv(2)(p21q31) associated with isolated bilateral microphthalmia and cataracts.

Weaver RG, Rao N, Thomas IT, Pettenati MJ. Weaver RG, et al. Among authors: rao n. Am J Med Genet. 1991 Sep 15;40(4):509-12. doi: 10.1002/ajmg.1320400428. Am J Med Genet. 1991. PMID: 1746620 Review.

7

Presenting characteristics of trisomy 8 as the primary cytogenetic abnormality associated with childhood acute lymphoblastic leukemia. A Pediatric Oncology Group (POG) Study (8600/8493).

Pettenati MJ, Rao N, Wofford M, Shuster JJ, Pullen DJ, Ling MP, Steuber CP, Carroll AJ. Pettenati MJ, et al. Among authors: rao n. Cancer Genet Cytogenet. 1994 Jul 1;75(1):6-10. doi: 10.1016/0165-4608(94)90208-9. Cancer Genet Cytogenet. 1994. PMID: 8039165

8

In situ localization of the genetic locus encoding the lysosomal acid lipase/cholesteryl esterase (LIPA) deficient in Wolman disease to chromosome 10q23.2-q23.3.

Anderson RA, Rao N, Byrum RS, Rothschild CB, Bowden DW, Hayworth R, Pettenati M. Anderson RA, et al. Among authors: rao n. Genomics. 1993 Jan;15(1):245-7. doi: 10.1006/geno.1993.1052. Genomics. 1993. PMID: 8432549 No abstract available.

9

Molecular characterization of a third member of the guanylyl cyclase-activating protein subfamily.

Haeseleer F, Sokal I, Li N, Pettenati M, Rao N, Bronson D, Wechter R, Baehr W, Palczewski K. Haeseleer F, et al. Among authors: rao n. J Biol Chem. 1999 Mar 5;274(10):6526-35. doi: 10.1074/jbc.274.10.6526. J Biol Chem. 1999. PMID: 10037746 Free article.

10

45,X/47,XYY mosaicism: clinical discrepancy between prenatally and postnatally diagnosed cases.

Pettenati MJ, Wheeler M, Bartlett DJ, Subrt I, Rao N, Kroovand RL, Burton BK, Kahler S, Park HK, Cosper P, et al. Pettenati MJ, et al. Among authors: rao n. Am J Med Genet. 1991 Apr 1;39(1):42-7. doi: 10.1002/ajmg.1320390111. Am J Med Genet. 1991. PMID: 1867264

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