Coerdt W - Search Results

1

Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies.

Southgate L, Sukalo M, Karountzos ASV, Taylor EJ, Collinson CS, Ruddy D, Snape KM, Dallapiccola B, Tolmie JL, Joss S, Brancati F, Digilio MC, Graul-Neumann LM, Salviati L, Coerdt W, Jacquemin E, Wuyts W, Zenker M, Machado RD, Trembath RC. Southgate L, et al. Among authors: coerdt w. Circ Cardiovasc Genet. 2015 Aug;8(4):572-581. doi: 10.1161/CIRCGENETICS.115.001086. Epub 2015 May 11. Circ Cardiovasc Genet. 2015. PMID: 25963545 Free PMC article.

2

Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception.

Zechner U, Pliushch G, Schneider E, El Hajj N, Tresch A, Shufaro Y, Seidmann L, Coerdt W, Müller AM, Haaf T. Zechner U, et al. Among authors: coerdt w. Mol Hum Reprod. 2010 Sep;16(9):704-13. doi: 10.1093/molehr/gap107. Epub 2009 Dec 9. Mol Hum Reprod. 2010. PMID: 20007506

3

Extreme methylation values of imprinted genes in human abortions and stillbirths.

Pliushch G, Schneider E, Weise D, El Hajj N, Tresch A, Seidmann L, Coerdt W, Müller AM, Zechner U, Haaf T. Pliushch G, et al. Among authors: coerdt w. Am J Pathol. 2010 Mar;176(3):1084-90. doi: 10.2353/ajpath.2010.090764. Epub 2010 Jan 21. Am J Pathol. 2010. PMID: 20093482 Free PMC article.

4

Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.

Schneider E, Pliushch G, El Hajj N, Galetzka D, Puhl A, Schorsch M, Frauenknecht K, Riepert T, Tresch A, Müller AM, Coerdt W, Zechner U, Haaf T. Schneider E, et al. Among authors: coerdt w. Nucleic Acids Res. 2010 Jul;38(12):3880-90. doi: 10.1093/nar/gkq126. Epub 2010 Mar 1. Nucleic Acids Res. 2010. PMID: 20194112 Free PMC article.

5

[Appendicitis in childhood: correlation of clinical data with histopathological findings].

Müller AM, Kaucevic M, Coerdt W, Turial S. Müller AM, et al. Among authors: coerdt w. Klin Padiatr. 2010 Dec;222(7):449-54. doi: 10.1055/s-0030-1263153. Epub 2010 Sep 9. Klin Padiatr. 2010. PMID: 20830659 German.

6

Interstitial deletion of the short arm of chromosome 3. Fetal pathology and exclusion of the gene for beta-galactosidase-1 (GLB-1) from 3(p11----p14.2).

Hertz JM, Coerdt W, Hahnemann N, Schwartz M. Hertz JM, et al. Among authors: coerdt w. Hum Genet. 1988 Aug;79(4):389-91. doi: 10.1007/BF00282185. Hum Genet. 1988. PMID: 3137147

7

Pectus excavatum: history, hypotheses and treatment options.

Brochhausen C, Turial S, Müller FK, Schmitt VH, Coerdt W, Wihlm JM, Schier F, Kirkpatrick CJ. Brochhausen C, et al. Among authors: coerdt w. Interact Cardiovasc Thorac Surg. 2012 Jun;14(6):801-6. doi: 10.1093/icvts/ivs045. Epub 2012 Mar 5. Interact Cardiovasc Thorac Surg. 2012. PMID: 22394989 Free PMC article. Review.

8

Down's syndrome in the male. Reproductive pathology and meiotic studies.

Johannisson R, Gropp A, Winking H, Coerdt W, Rehder H, Schwinger E. Johannisson R, et al. Among authors: coerdt w. Hum Genet. 1983;63(2):132-8. doi: 10.1007/BF00291532. Hum Genet. 1983. PMID: 6220959

9

Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions?

Rehder H, Coerdt W, Eggers R, Klink F, Schwinger E. Rehder H, et al. Among authors: coerdt w. Hum Genet. 1989 Jul;82(4):377-85. doi: 10.1007/BF00274002. Hum Genet. 1989. PMID: 2737670

10

Isochromosome 18q with karyotype 46,XX,i(18q). Cytogenetics and pathology.

Froster-Iskenius U, Coerdt W, Rehder H, Schwinger E. Froster-Iskenius U, et al. Among authors: coerdt w. Clin Genet. 1984 Dec;26(6):549-54. doi: 10.1111/j.1399-0004.1984.tb01102.x. Clin Genet. 1984. PMID: 6499266

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