Sperling K - Search Results

1

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.

Saar K, Chrzanowska KH, Stumm M, Jung M, Nürnberg G, Wienker TF, Seemanová E, Wegner RD, Reis A, Sperling K. Saar K, et al. Among authors: sperling k. Am J Hum Genet. 1997 Mar;60(3):605-10. Am J Hum Genet. 1997. PMID: 9042920 Free PMC article.

2

Relative DNA content of human euchromatin and heterochromatin after G, C and Giemsa 11 banding.

Schmiady H, Wegner RD, Sperling K. Schmiady H, et al. Among authors: sperling k. Humangenetik. 1975 Aug 29;29(1):85-9. doi: 10.1007/BF00273354. Humangenetik. 1975. PMID: 51823

3

A simple staining technique to demonstrate chromosomal DNA replication.

Wegner RD, Sperling K. Wegner RD, et al. Among authors: sperling k. Experientia. 1976 Sep 15;32(9):1220-1. doi: 10.1007/BF01927637. Experientia. 1976. PMID: 61135

4

Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12-q21.

Reis A, Küster W, Eckardt R, Sperling K. Reis A, et al. Among authors: sperling k. Hum Genet. 1992 Sep-Oct;90(1-2):113-6. doi: 10.1007/BF00210752. Hum Genet. 1992. PMID: 1385292

5

Frequency of trisomy 21 in Germany before and after the Chernobyl accident.

Sperling K, Pelz J, Wegner RD, Schulzke I, Struck E. Sperling K, et al. Biomed Pharmacother. 1991;45(6):255-62. doi: 10.1016/0753-3322(91)90026-p. Biomed Pharmacother. 1991. PMID: 1832977

6

Frequency of the delta F508 mutation and flanking marker haplotypes at the CF locus from 167 Czech families.

Macek M Jr, Vavrová V, Böhm I, Stuhrmann M, Reis A, Duspivová R, Macek M, Sperling K, Krawczak M, Schmidtke J. Macek M Jr, et al. Among authors: sperling k. Hum Genet. 1990 Sep;85(4):417-8. doi: 10.1007/BF02428289. Hum Genet. 1990. PMID: 2210755

7

DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations.

Nürnberg P, Roewer L, Neitzel H, Sperling K, Pöpperl A, Hundrieser J, Pöche H, Epplen C, Zischler H, Epplen JT. Nürnberg P, et al. Among authors: sperling k. Hum Genet. 1989 Dec;84(1):75-8. doi: 10.1007/BF00210676. Hum Genet. 1989. PMID: 2558069

8

A new chromosomal instability disorder confirmed by complementation studies.

Wegner RD, Metzger M, Hanefeld F, Jaspers NG, Baan C, Magdorf K, Kunze J, Sperling K. Wegner RD, et al. Among authors: sperling k. Clin Genet. 1988 Jan;33(1):20-32. Clin Genet. 1988. PMID: 3277755 Review.

9

Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response.

Digweed M, Zakrzewski-Lüdcke S, Sperling K. Digweed M, et al. Among authors: sperling k. Hum Genet. 1988 Jan;78(1):51-4. doi: 10.1007/BF00291234. Hum Genet. 1988. PMID: 3338794

10

Trisomy 14 mosaicism leading to cytogenetic discrepancies in chorionic villi sampled at different times.

Wegner RD, Hohle R, Karkut G, Sperling K. Wegner RD, et al. Among authors: sperling k. Prenat Diagn. 1988 Mar;8(3):239-43. doi: 10.1002/pd.1970080311. Prenat Diagn. 1988. PMID: 3375201

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