Diehl SR - Search Results

1

Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line.

Reynolds JE, Fletcher JA, Lytle CH, Nie L, Morton CC, Diehl SR. Reynolds JE, et al. Among authors: diehl sr. Hum Genet. 1992 Dec;90(4):450-6. doi: 10.1007/BF00220476. Hum Genet. 1992. PMID: 1483704

2

Dinucleotide repeat polymorphism at the CHRND locus.

Landa BL, Reynolds JE, Beeson D, Diehl SR. Landa BL, et al. Among authors: diehl sr. Hum Mol Genet. 1994 Aug;3(8):1445. doi: 10.1093/hmg/3.8.1445. Hum Mol Genet. 1994. PMID: 7987343 No abstract available.

3

A method for recovery of high-molecular-weight DNA suitable for field-inversion gel electrophoresis from frozen tumor cells.

Reynolds JE, Diehl SR. Reynolds JE, et al. Among authors: diehl sr. Cancer Genet Cytogenet. 1993 Jan;65(1):68-70. doi: 10.1016/0165-4608(93)90061-p. Cancer Genet Cytogenet. 1993. PMID: 8431917

4

Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome.

Reynolds JE, Marazita ML, Meyer JM, Stevens CA, Eaves LJ, Arnos KS, Ploughman LM, MacLean C, Nance WE, Diehl SR. Reynolds JE, et al. Among authors: diehl sr. Am J Hum Genet. 1996 Feb;58(2):384-92. Am J Hum Genet. 1996. PMID: 8571965 Free PMC article.

5

Analysis of variability of clinical manifestations in Waardenburg syndrome.

Reynolds JE, Meyer JM, Landa B, Stevens CA, Arnos KS, Israel J, Marazita ML, Bodurtha J, Nance WE, Diehl SR. Reynolds JE, et al. Among authors: diehl sr. Am J Med Genet. 1995 Jul 17;57(4):540-7. doi: 10.1002/ajmg.1320570405. Am J Med Genet. 1995. PMID: 7573125

6

Abnormal regulation of mammalian p21ras contributes to malignant tumor growth in von Recklinghausen (type 1) neurofibromatosis.

DeClue JE, Papageorge AG, Fletcher JA, Diehl SR, Ratner N, Vass WC, Lowy DR. DeClue JE, et al. Among authors: diehl sr. Cell. 1992 Apr 17;69(2):265-73. doi: 10.1016/0092-8674(92)90407-4. Cell. 1992. PMID: 1568246

7

A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene.

Diehl SR, Boehnke M, Erickson RP, Ploughman LM, Seiler KA, Lieberman JL, Clarke HB, Bruce MA, Schorry EK, Pericak-Vance M, et al. Diehl SR, et al. Am J Hum Genet. 1989 Jan;44(1):33-7. Am J Hum Genet. 1989. PMID: 2491779 Free PMC article.

8

Reevaluation of the chromosome 4q candidate region for early onset periodontitis.

Hart TC, Marazita ML, McCanna KM, Schenkein HA, Diehl SR. Hart TC, et al. Among authors: diehl sr. Hum Genet. 1993 Jun;91(5):416-22. doi: 10.1007/BF00217764. Hum Genet. 1993. PMID: 8100208

9

Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8.

Diehl SR, Boehnke M, Collins FS, Erickson RP, Karolyi IJ, Ploughman LM, Pericak-Vance MA, Aylsworth AS, Roses AD. Diehl SR, et al. J Med Genet. 1987 Sep;24(9):532-4. doi: 10.1136/jmg.24.9.532. J Med Genet. 1987. PMID: 3118034 Free PMC article.

10

Application of automated DNA sizing technology for genotyping microsatellite loci.

Ziegle JS, Su Y, Corcoran KP, Nie L, Mayrand PE, Hoff LB, McBride LJ, Kronick MN, Diehl SR. Ziegle JS, et al. Among authors: diehl sr. Genomics. 1992 Dec;14(4):1026-31. doi: 10.1016/s0888-7543(05)80126-0. Genomics. 1992. PMID: 1478644

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