Papenhausen PN - Search Results

1

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.

Huang B, Crolla JA, Christian SL, Wolf-Ledbetter ME, Macha ME, Papenhausen PN, Ledbetter DH. Huang B, et al. Among authors: papenhausen pn. Hum Genet. 1997 Jan;99(1):11-7. doi: 10.1007/s004390050301. Hum Genet. 1997. PMID: 9003485

2

Tissue limited mosaicism in a patient with tetrasomy 9p.

Papenhausen P, Riscile G, Miller K, Kousseff B, Tedesco T. Papenhausen P, et al. Am J Med Genet. 1990 Nov;37(3):388-91. doi: 10.1002/ajmg.1320370319. Am J Med Genet. 1990. PMID: 2260570

3

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.

Ravnan JB, Tepperberg JH, Papenhausen P, Lamb AN, Hedrick J, Eash D, Ledbetter DH, Martin CL. Ravnan JB, et al. J Med Genet. 2006 Jun;43(6):478-89. doi: 10.1136/jmg.2005.036350. Epub 2005 Sep 30. J Med Genet. 2006. PMID: 16199540 Free PMC article.

4

Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities.

Schröck E, Veldman T, Padilla-Nash H, Ning Y, Spurbeck J, Jalal S, Shaffer LG, Papenhausen P, Kozma C, Phelan MC, Kjeldsen E, Schonberg SA, O'Brien P, Biesecker L, du Manoir S, Ried T. Schröck E, et al. Hum Genet. 1997 Dec;101(3):255-62. doi: 10.1007/s004390050626. Hum Genet. 1997. PMID: 9439652

5

Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.

Levy B, Papenhausen P, Tepperberg J, Dunn T, Fallet S, Magid M, Kardon N, Hirschhorn K, Warburton P. Levy B, et al. Cytogenet Cell Genet. 2000;91(1-4):165-70. doi: 10.1159/000056839. Cytogenet Cell Genet. 2000. PMID: 11173851

6

Inv(16) occurring in a case of acute biphenotypic leukemia lacking monocytic markers: multiple but short remissions.

Paietta E, Papenhausen P, Azar C, Wiernik PH, Spielvogel A. Paietta E, et al. Cancer Genet Cytogenet. 1987 Apr;25(2):367-8. doi: 10.1016/0165-4608(87)90199-3. Cancer Genet Cytogenet. 1987. PMID: 3470123 No abstract available.

7

Cleft palate and complex chromosome rearrangements.

Kousseff BG, Papenhausen P, Neu RL, Essig YP, Saraceno CA. Kousseff BG, et al. Clin Genet. 1992 Sep;42(3):135-42. doi: 10.1111/j.1399-0004.1992.tb03225.x. Clin Genet. 1992. PMID: 1327590 Review.

8

Translocation t(12;19)(q13;q13.3). A new recurrent abnormality in acute nonlymphocytic leukemia with atypical erythropoiesis.

Paietta E, Papenhausen P, Gucalp R, Wiernik PH. Paietta E, et al. Cancer Genet Cytogenet. 1988 Aug;34(1):19-23. doi: 10.1016/0165-4608(88)90162-8. Cancer Genet Cytogenet. 1988. PMID: 3395990

9

Philadelphia chromosome positive essential thrombocythemia evolving into lymphoid blast crisis.

Paietta E, Rosen N, Roberts M, Papenhausen P, Wiernik PH. Paietta E, et al. Cancer Genet Cytogenet. 1987 Apr;25(2):227-31. doi: 10.1016/0165-4608(87)90182-8. Cancer Genet Cytogenet. 1987. PMID: 3470113

10

Biphenotypic leukemia with unusual chromosomal translocation in a patient treated for melanoma.

Paietta E, Papenhausen P, Ciobanu N, Dutcher JP, Wiernik PH. Paietta E, et al. Cancer Genet Cytogenet. 1986 Apr 15;21(4):355-60. doi: 10.1016/0165-4608(86)90217-7. Cancer Genet Cytogenet. 1986. PMID: 2937529

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