Lindeman R - Search Results

1

Molecular and cytogenetic studies of the Prader-Willi syndrome.

Trent RJ, Volpato F, Smith A, Lindeman R, Wong MK, Warne G, Haan E. Trent RJ, et al. Among authors: lindeman r. J Med Genet. 1991 Oct;28(10):649-54. doi: 10.1136/jmg.28.10.649. J Med Genet. 1991. PMID: 1682493 Free PMC article.

2

Dinucleotide repeat polymorphism of D15S10 in the Prader-Willi chromosome region (PWCR).

Lindeman R, Kouts S, Woodage T, Smith A, Trent RJ. Lindeman R, et al. Nucleic Acids Res. 1991 Oct 11;19(19):5449. doi: 10.1093/nar/19.19.5449-a. Nucleic Acids Res. 1991. PMID: 1923838 Free PMC article. No abstract available.

3

A de novo unbalanced reciprocal translocation identified as paternal in origin in the Prader-Willi syndrome.

Smith A, Lindeman R, Volpato F, Kearney A, White S, Haan E, Trent RJ. Smith A, et al. Among authors: lindeman r. Hum Genet. 1991 Mar;86(5):534-6. doi: 10.1007/BF00194651. Hum Genet. 1991. PMID: 2016095

4

A variety of genetic mechanisms are associated with the Prader-Willi syndrome.

Woodage T, Deng ZM, Prasad M, Smart R, Lindeman R, Christian SL, Ledbetter DH, Robson L, Smith A, Trent RJ. Woodage T, et al. Among authors: lindeman r. Am J Med Genet. 1994 Sep 15;54(3):219-26. doi: 10.1002/ajmg.1320540308. Am J Med Genet. 1994. PMID: 7810579

5

Physical mapping studies at D15S10: implications for candidate gene identification in the Angelman syndrome/Prader-Willi syndrome chromosome region of 15q11-q13.

Woodage T, Lindeman R, Deng ZM, Fimmel A, Smith A, Trent RJ. Woodage T, et al. Among authors: lindeman r. Genomics. 1994 Jan 1;19(1):170-2. doi: 10.1006/geno.1994.1031. Genomics. 1994. PMID: 8188222

6

Australian beta zero-thalassaemia: a high haemoglobin A2 beta zero-thalassaemia due to a 12 kb deletion commencing 5' to the beta-globin gene.

Motum PI, Lindeman R, Hamilton TJ, Trent RJ. Motum PI, et al. Among authors: lindeman r. Br J Haematol. 1992 Sep;82(1):107-13. doi: 10.1111/j.1365-2141.1992.tb04601.x. Br J Haematol. 1992. PMID: 1419783

7

Polymerase chain reaction (PCR) mutagenesis enabling rapid non-radioactive detection of common beta-thalassaemia mutations in Mediterraneans.

Lindeman R, Hu SP, Volpato F, Trent RJ. Lindeman R, et al. Br J Haematol. 1991 May;78(1):100-4. doi: 10.1111/j.1365-2141.1991.tb04389.x. Br J Haematol. 1991. PMID: 1675115

8

Experience of a molecular genetics service in prenatal diagnosis by DNA analysis.

Trent RJ, Volpato F, Wallace RC, Lindeman R, Yakas J. Trent RJ, et al. Among authors: lindeman r. Pathology. 1990 Jul;22(3):165-8. doi: 10.3109/00313029009063558. Pathology. 1990. PMID: 2243730

9

Molecular characterisation of Vietnamese HPFH.

Motum PI, Hamilton TJ, Lindeman R, Le H, Trent RJ. Motum PI, et al. Among authors: lindeman r. Hum Mutat. 1993;2(3):179-84. doi: 10.1002/humu.1380020305. Hum Mutat. 1993. PMID: 7689901

10

Utility of the polymerase chain reaction (PCR) for prenatal diagnosis of genetic disease.

Lindeman R, Wallace R, Volpato F, Hu SP, Trent RJ. Lindeman R, et al. Pathology. 1991 Apr;23(2):158-63. doi: 10.3109/00313029109060817. Pathology. 1991. PMID: 1745568

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