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Two cases of prenatally diagnosed diaphragmatic hernia accompanied by the same undescribed chromosomal deletion (15q24 de novo).
Bettelheim D, Hengstschläger M, Drahonsky R, Eppel W, Bernaschek G. Bettelheim D, et al. Among authors: hengstschlager m. Clin Genet. 1998 Apr;53(4):319-20. doi: 10.1111/j.1399-0004.1998.tb02706.x. Clin Genet. 1998. PMID: 9650775 No abstract available.
Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: a new case and discussion of the literature.
Hengstschläger M, Mittermayer C, Repa C, Drahonsky R, Deutinger J, Bernaschek G. Hengstschläger M, et al. Fetal Diagn Ther. 2004 Nov-Dec;19(6):510-2. doi: 10.1159/000080164. Fetal Diagn Ther. 2004. PMID: 15539876 Review.
Raising the sensitivity of fetal RhD typing and sex determination from maternal blood.
Hengstschläger M, Hölzl G, Ulm B, Bernaschek G. Hengstschläger M, et al. J Med Genet. 1997 Apr;34(4):350-1. doi: 10.1136/jmg.34.4.350-b. J Med Genet. 1997. PMID: 9138165 Free PMC article. No abstract available.
Tuberous sclerosis gene products in proliferation control.
Hengstschläger M, Rodman DM, Miloloza A, Hengstschläger-Ottnad E, Rosner M, Kubista M. Hengstschläger M, et al. Among authors: hengstschlager ottnad e. Mutat Res. 2001 Jul;488(3):233-9. doi: 10.1016/s1383-5742(01)00058-8. Mutat Res. 2001. PMID: 11397651 Review.
Stem cell marker expression in human trisomy 21 amniotic fluid cells and trophoblasts.
Prusa AR, Marton E, Rosner M, Freilinger A, Bernaschek G, Hengstschläger M. Prusa AR, et al. Among authors: hengstschlager m. J Neural Transm Suppl. 2003;(67):235-42. doi: 10.1007/978-3-7091-6721-2_21. J Neural Transm Suppl. 2003. PMID: 15068255
Prenatal diagnosis and postmortem study of a fetus with de novo dup (2) (q11-q21). A new case.
Golaszewski T, Hengstschläger M, Frigo P, Prayer D, Urbanits S, Bernaschek G. Golaszewski T, et al. Among authors: hengstschlager m. Acta Obstet Gynecol Scand. 1998 Oct;77(9):935-6. doi: 10.1034/j.1600-0412.1998.770912.x. Acta Obstet Gynecol Scand. 1998. PMID: 9808384 No abstract available.
Role of the tuberous sclerosis gene-2 product in cell cycle control. Loss of the tuberous sclerosis gene-2 induces quiescent cells to enter S phase.
Soucek T, Pusch O, Wienecke R, DeClue JE, Hengstschläger M. Soucek T, et al. Among authors: hengstschlager m. J Biol Chem. 1997 Nov 14;272(46):29301-8. doi: 10.1074/jbc.272.46.29301. J Biol Chem. 1997. PMID: 9361010
Genetic disorders in premature ovarian failure.
Laml T, Preyer O, Umek W, Hengstschlager M, Hanzal H. Laml T, et al. Among authors: hengstschlager m. Hum Reprod Update. 2002 Sep-Oct;8(5):483-91. doi: 10.1093/humupd/8.5.483. Hum Reprod Update. 2002. PMID: 12398227 Review.
Fetal cells in the peripheral blood of pregnant women express thymidine kinase: a new marker for detection.
Hengstschläger M, Bernaschek G. Hengstschläger M, et al. FEBS Lett. 1997 Mar 10;404(2-3):299-302. doi: 10.1016/s0014-5793(97)00144-0. FEBS Lett. 1997. PMID: 9119083
Genetic factors in assisted reproduction.
Gruber CJ, Hengstschläger M, Leipold H, Gruber IM, Ferlitsch K, Gruber DM, Huber JC. Gruber CJ, et al. Among authors: hengstschlager m. Wien Klin Wochenschr. 2003 Dec 15;115(23):805-11. doi: 10.1007/BF03041040. Wien Klin Wochenschr. 2003. PMID: 14740343 Review.
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