Haas O - Search Results

1

Constitutional chromosome anomalies in patients with cerebral gigantism (Sotos syndrome).

Haeusler G, Guchev Z, Köhler I, Schober E, Haas O, Frisch H. Haeusler G, et al. Among authors: haas o. Klin Padiatr. 1993 Sep-Oct;205(5):351-3. doi: 10.1055/s-2007-1025247. Klin Padiatr. 1993. PMID: 8411901

2

[Wiedemann-Beckwith syndrome: clinical characteristics, constitutional chromosome abnormalities and tumor incidence].

Haas OA, Zoubek A, Grümayer ER, Ferstl G, Gadner H. Haas OA, et al. Klin Padiatr. 1987 Jul-Aug;199(4):283-91. doi: 10.1055/s-2008-1026804. Klin Padiatr. 1987. PMID: 2821320 German.

3

Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature.

Fischer H, Oswald HP, Duba HC, Doczy L, Simma B, Utermann G, Haas OA. Fischer H, et al. Among authors: haas oa. Klin Padiatr. 1993 May-Jun;205(3):162-6. Klin Padiatr. 1993. PMID: 8350589 Review.

4

Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosome.

Birnbacher R, Chudoba I, Pirc-Danoewinata H, König M, Kohlhauser C, Schnedl W, Haas OA. Birnbacher R, et al. Among authors: haas oa. Ann Genet. 2001 Jan-Mar;44(1):13-8. doi: 10.1016/s0003-3995(00)01033-9. Ann Genet. 2001. PMID: 11334612 Review.

5

Concurrent FOXP3- and CTLA4-associated genetic predisposition and skewed X chromosome inactivation in an autoimmune disease-prone family.

Seidel MG, Rami B, Item C, Schober E, Zeitlhofer P, Huber WD, Heitger A, Bodamer OA, Haas OA. Seidel MG, et al. Among authors: haas oa. Eur J Endocrinol. 2012 Jul;167(1):131-4. doi: 10.1530/EJE-12-0197. Epub 2012 Mar 26. Eur J Endocrinol. 2012. PMID: 22450550

6

Minimal residual disease-based treatment is adequate for relapse-prone childhood acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21: the experience of the ALL-BFM 2000 trial.

Attarbaschi A, Panzer-Grümayer R, Mann G, Möricke A, König M, Mecklenbräuker A, Teigler-Schlegel A, Bradtke J, Harbott J, Göhring G, Stanulla M, Schrappe M, Zimmermann M, Haas OA; Austrian and German ALL-BFM (Berlin-Frankfurt-Münster) Study Group. Attarbaschi A, et al. Among authors: haas oa. Klin Padiatr. 2014 Nov;226(6-7):338-43. doi: 10.1055/s-0034-1387795. Epub 2014 Nov 28. Klin Padiatr. 2014. PMID: 25431866 Clinical Trial.

7

Acute megakaryocytic leukemia in children. Clinical, immunologic, and cytogenetic findings in two patients.

Slavc I, Urban C, Haas OA, Kroisel PM, Köller U. Slavc I, et al. Among authors: haas oa. Cancer. 1991 Nov 15;68(10):2266-72. doi: 10.1002/1097-0142(19911115)68:10<2266::aid-cncr2820681027>3.0.co;2-b. Cancer. 1991. PMID: 1833041 Review.

8

Translocation (16;21)(p11;q22) in acute monoblastic leukemia with erythrophagocytosis.

Marosi C, Bettelheim P, Geissler K, Lechner K, Köller U, Haas OA, Chott A, Hagemeijer A. Marosi C, et al. Among authors: haas oa. Cancer Genet Cytogenet. 1991 Jul 1;54(1):61-6. doi: 10.1016/0165-4608(91)90030-x. Cancer Genet Cytogenet. 1991. PMID: 2065316

9

Trisomy 4: a specific karyotype anomaly in primary and secondary acute myeloid leukemia.

Weber E, Nowotny H, Haas OA, Kasparu H, Grois N, Lutz D. Weber E, et al. Among authors: haas oa. Leukemia. 1990 Mar;4(3):219-21. Leukemia. 1990. PMID: 2179639 Review.

10

Phenotypic and genotypic heterogeneity in infant acute leukemia. II. Acute nonlymphoblastic leukemia.

Köller U, Haas OA, Ludwig WD, Bartram CR, Harbott J, Panzer-Grümayer R, Hansen-Hagge T, Ritter J, Creutzig U, Knapp W, et al. Köller U, et al. Among authors: haas oa. Leukemia. 1989 Oct;3(10):708-14. Leukemia. 1989. PMID: 2779287

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

457 results

Search Page

Filters