Nöthen MM - Search Results

1

Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction.

Eggermann T, Nöthen MM, Eiben B, Hofmann D, Hinkel K, Fimmers R, Schwanitz G. Eggermann T, et al. Among authors: nothen mm. Hum Genet. 1996 Feb;97(2):218-23. doi: 10.1007/BF02265269. Hum Genet. 1996. PMID: 8566957

2

Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder.

Nöthen MM, Erdmann J, Körner J, Lanczik M, Fritze J, Fimmers R, Grandy DK, O'Dowd B, Propping P. Nöthen MM, et al. Am J Psychiatry. 1992 Feb;149(2):199-201. doi: 10.1176/ajp.149.2.199. Am J Psychiatry. 1992. PMID: 1346486

3

Dinucleotide repeat polymorphism at the human CD59 locus.

Nöthen MM, Dewald G. Nöthen MM, et al. Clin Genet. 1995 Mar;47(3):165-6. doi: 10.1111/j.1399-0004.1995.tb03952.x. Clin Genet. 1995. PMID: 7543386 No abstract available.

4

Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls.

Körner J, Rietschel M, Hunt N, Castle D, Gill M, Nöthen MM, Craddock N, Daniels J, Owen M, Fimmers R, et al. Körner J, et al. Among authors: nothen mm. Psychiatr Genet. 1994 Fall;4(3):167-75. doi: 10.1097/00041444-199400430-00007. Psychiatr Genet. 1994. PMID: 7719703

5

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.

Nöthen MM, Cichon S, Hemmer S, Hebebrand J, Remschmidt H, Lehmkuhl G, Poustka F, Schmidt M, Catalano M, Fimmers R, et al. Nöthen MM, et al. Hum Mol Genet. 1994 Dec;3(12):2207-12. doi: 10.1093/hmg/3.12.2207. Hum Mol Genet. 1994. PMID: 7881421

6

Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomes.

Viersbach R, Schwanitz G, Nöthen MM. Viersbach R, et al. Among authors: nothen mm. Hum Genet. 1994 Jun;93(6):663-7. doi: 10.1007/BF00201567. Hum Genet. 1994. PMID: 8005590

7

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).

Cichon S, Nöthen MM, Erdmann J, Propping P. Cichon S, et al. Among authors: nothen mm. Hum Mol Genet. 1994 Jan;3(1):209. doi: 10.1093/hmg/3.1.209. Hum Mol Genet. 1994. PMID: 8162032 No abstract available.

8

A common amino acid polymorphism in complement component C1R.

Nöthen MM, Dewald G. Nöthen MM, et al. Hum Mol Genet. 1994 Jan;3(1):217. doi: 10.1093/hmg/3.1.217-a. Hum Mol Genet. 1994. PMID: 8162045 No abstract available.

9

Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling.

Eggermann T, Nöthen MM, Propping P, Schwanitz G. Eggermann T, et al. Among authors: nothen mm. Ann Genet. 1993;36(4):214-6. Ann Genet. 1993. PMID: 8166427

10

The use of microsatellites in zygosity diagnosis of twins.

Erdmann J, Nöthen MM, Stratmann M, Fimmers R, Franzek E, Propping P. Erdmann J, et al. Among authors: nothen mm. Acta Genet Med Gemellol (Roma). 1993;42(1):45-51. doi: 10.1017/s0515283600042281. Acta Genet Med Gemellol (Roma). 1993. PMID: 8191861

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