Rehder H - Search Results

1

Clinical and cytogenetic studies in a large (4;8) translocation family with pre- and postnatal Wolf syndrome.

Tranebjaerg L, Petersen A, Hove K, Rehder H, Mikkelsen M. Tranebjaerg L, et al. Among authors: rehder h. Ann Genet. 1984;27(4):224-9. Ann Genet. 1984. PMID: 6335368

2

Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.

Dietze I, Fritz B, Huhle D, Simoens W, Piecha E, Rehder H. Dietze I, et al. Among authors: rehder h. Fetal Diagn Ther. 2004 May-Jun;19(3):251-60. doi: 10.1159/000076707. Fetal Diagn Ther. 2004. PMID: 15067236 Review.

3

Familial cryptic translocation with del 4q34-->qter and dup 12pter-->p13 in sibs with tracheal stenosis: clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimen.

Fritz B, Greber-Platzer S, Frischer T, Streubel B, Gröblacher J, Amann G, Ventruba P, Rehder H, Fonatsch C. Fritz B, et al. Among authors: rehder h. Am J Med Genet. 2000 Oct 2;94(4):271-80. doi: 10.1002/1096-8628(20001002)94:4<271::aid-ajmg2>3.0.co;2-y. Am J Med Genet. 2000. PMID: 11038438

4

Partial trisomy 1q syndrome.

Rehder H, Friedrich U. Rehder H, et al. Clin Genet. 1979 Jun;15(6):534-40. doi: 10.1111/j.1399-0004.1979.tb00838.x. Clin Genet. 1979. PMID: 466853

5

Proliferation kinetics of chorionic villi in chromosomally normal and abnormal spontaneous abortions analyzed by premature chromosome condensation and northern blot.

Miller K, Metze V, Wang R, Lin X, Rehder H. Miller K, et al. Among authors: rehder h. Ann Genet. 1996;39(3):159-67. Ann Genet. 1996. PMID: 8839889

6

Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel-Manzke syndrome in a fetus.

Schoner K, Bald R, Horn D, Rehder H, Kornak U, Ehmke N. Schoner K, et al. Among authors: rehder h. Am J Med Genet A. 2017 Jun;173(6):1694-1697. doi: 10.1002/ajmg.a.38209. Epub 2017 Apr 19. Am J Med Genet A. 2017. PMID: 28422407

7

Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.

Wieser R, Fritz B, Ullmann R, Müller I, Galhuber M, Storlazzi CT, Ramaswamy A, Christiansen H, Shimizu N, Rehder H. Wieser R, et al. Among authors: rehder h. Hum Mutat. 2005 Aug;26(2):78-83. doi: 10.1002/humu.20195. Hum Mutat. 2005. PMID: 15957176

8

Tetrasomy 12p (Pallister-Killian syndrome): difficulties in prenatal diagnosis.

Kunz J, Schoner K, Stein W, Rehder H, Fritz B. Kunz J, et al. Among authors: rehder h. Arch Gynecol Obstet. 2009 Dec;280(6):1049-53. doi: 10.1007/s00404-009-1059-3. Epub 2009 Apr 2. Arch Gynecol Obstet. 2009. PMID: 19340439

9

Chromosome mosaicism of the placenta--a cause of developmental failure of the fetus?

Schwinger E, Seidl E, Klink F, Rehder H. Schwinger E, et al. Among authors: rehder h. Prenat Diagn. 1989 Sep;9(9):639-47. doi: 10.1002/pd.1970090907. Prenat Diagn. 1989. PMID: 2798350

10

Variability in the phenotypic expression of fryns syndrome: A report of two sibships.

Ramsing M, Gillessen-Kaesbach G, Holzgreve W, Fritz B, Rehder H. Ramsing M, et al. Among authors: rehder h. Am J Med Genet. 2000 Dec 18;95(5):415-24. doi: 10.1002/1096-8628(20001218)95:5<415::aid-ajmg2>3.0.co;2-j. Am J Med Genet. 2000. PMID: 11146459

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