Schindler D - Search Results

1

Recurrent mutation pressure does not explain the prevalence of the marker (X) syndrome.

Vogel F, Krüger J, Nielsen KB, Fryns JP, Schindler D, Schinzel A, Schmidt A, Schwinger E. Vogel F, et al. Among authors: schindler d. Hum Genet. 1985;71(1):1-6. doi: 10.1007/BF00295657. Hum Genet. 1985. PMID: 3861564

2

Endogenous blockage and delay of the chromosome cycle despite normal recruitment and growth phase explain poor proliferation and frequent edomitosis in Fanconi anemia cells.

Kubbies M, Schindler D, Hoehn H, Schinzel A, Rabinovitch PS. Kubbies M, et al. Among authors: schindler d. Am J Hum Genet. 1985 Sep;37(5):1022-30. Am J Hum Genet. 1985. PMID: 4050789 Free PMC article.

3

Physical mapping of the holoprosencephaly critical region on chromosome 7q36.

Gurrieri F, Trask BJ, van den Engh G, Krauss CM, Schinzel A, Pettenati MJ, Schindler D, Dietz-Band J, Vergnaud G, Scherer SW, et al. Gurrieri F, et al. Among authors: schindler d. Nat Genet. 1993 Mar;3(3):247-51. doi: 10.1038/ng0393-247. Nat Genet. 1993. PMID: 8485580

4

Screening test for ataxia telangiectasia.

Schindler D, Seyschab H, Poot M, Hoehn H, Schinzel A, Fryns JP, Tommerup N, Rabinovitch PS. Schindler D, et al. Lancet. 1987 Dec 12;2(8572):1398-9. doi: 10.1016/s0140-6736(87)91288-8. Lancet. 1987. PMID: 2890980 No abstract available.

5

Confirmation of Fanconi's anemia and detection of a chromosomal aberration (1Q12-32 triplication) via BrdU/Hoechst flow cytometry.

Schindler D, Kubbies M, Hoehn H, Schinzel A, Rabinovitch PS. Schindler D, et al. Am J Pediatr Hematol Oncol. 1987 Summer;9(2):172-7. doi: 10.1097/00043426-198722000-00014. Am J Pediatr Hematol Oncol. 1987. PMID: 3592130

6

Presymptomatic diagnosis of Fanconi's anaemia.

Schindler D, Kubbies M, Hoehn H, Schinzel A, Rabinovitch PS. Schindler D, et al. Lancet. 1985 Apr 20;1(8434):937. doi: 10.1016/s0140-6736(85)91717-9. Lancet. 1985. PMID: 2858786 No abstract available.

7

Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes.

Seyschab H, Schindler D, Friedl R, Barbi G, Boltshauser E, Fryns JP, Hanefeld F, Korinthenberg R, Krägeloh-Mann I, Scheres JM, et al. Seyschab H, et al. Among authors: schindler d. Eur J Pediatr. 1992 Oct;151(10):756-60. doi: 10.1007/BF01959085. Eur J Pediatr. 1992. PMID: 1425798

8

Structure, origin and effects of a supernumerary marker chromosome 15.

Schmid M, Schindler D, Haaf T. Schmid M, et al. Among authors: schindler d. Clin Genet. 1986 Jul;30(1):63-71. doi: 10.1111/j.1399-0004.1986.tb00570.x. Clin Genet. 1986. PMID: 3463440

9

Fanconi anemia mutation causes cellular susceptibility to ambient oxygen.

Schindler D, Hoehn H. Schindler D, et al. Am J Hum Genet. 1988 Oct;43(4):429-35. Am J Hum Genet. 1988. PMID: 3177386 Free PMC article.

10

Localisation of a Fanconi anaemia gene to chromosome 9p.

Saar K, Schindler D, Wegner RD, Reis A, Wienker TF, Hoehn H, Joenje H, Sperling K, Digweed M. Saar K, et al. Among authors: schindler d. Eur J Hum Genet. 1998 Sep-Oct;6(5):501-8. doi: 10.1038/sj.ejhg.5200241. Eur J Hum Genet. 1998. PMID: 9801875

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