Schwinger E - Search Results

1

Fra(X) frequency on the active X-chromosome and phenotype in heterozygous carriers of the fra(X) form of mental retardation.

Wilhelm D, Froster-Iskenius U, Paul J, Schwinger E. Wilhelm D, et al. Among authors: schwinger e. Am J Med Genet. 1988 May-Jun;30(1-2):407-15. doi: 10.1002/ajmg.1320300141. Am J Med Genet. 1988. PMID: 3177461

2

Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q).

Paul J, Froster-Iskenius U, Moje W, Schwinger E. Paul J, et al. Among authors: schwinger e. Hum Genet. 1984;66(4):344-6. doi: 10.1007/BF00287638. Hum Genet. 1984. PMID: 6586635

3

Folic acid treatment in males and females with fragile-(X)-syndrome.

Froster-Iskenius U, Bödeker K, Oepen T, Matthes R, Piper U, Schwinger E. Froster-Iskenius U, et al. Among authors: schwinger e. Am J Med Genet. 1986 Jan-Feb;23(1-2):273-89. doi: 10.1002/ajmg.1320230121. Am J Med Genet. 1986. PMID: 3513569 Clinical Trial.

4

Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study.

Rodewald A, Froster-Iskenius U, Käb E, Langenbeck U, Schinzel A, Schmidt A, Schwinger E, Steinbach P, Veenema H, Wegner RD, et al. Rodewald A, et al. Among authors: schwinger e. Clin Genet. 1986 Jul;30(1):1-13. doi: 10.1111/j.1399-0004.1986.tb00563.x. Clin Genet. 1986. PMID: 3757292

5

Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large families.

Froster-Iskenius U, Schulze A, Schwinger E. Froster-Iskenius U, et al. Among authors: schwinger e. Hum Genet. 1984;67(4):419-27. doi: 10.1007/BF00291403. Hum Genet. 1984. PMID: 6593289

6

Screening for fra(X)(q) in a population of mentally retarded males.

Froster-Iskenius U, Felsch G, Schirren C, Schwinger E. Froster-Iskenius U, et al. Among authors: schwinger e. Hum Genet. 1983;63(2):153-7. doi: 10.1007/BF00291535. Hum Genet. 1983. PMID: 6682403

7

Replication pattern in XXY cells with fra(X).

Froster-Iskenius U, Schwinger E, Weigert M, Fonatsch C. Froster-Iskenius U, et al. Among authors: schwinger e. Hum Genet. 1982;60(3):278-80. doi: 10.1007/BF00303019. Hum Genet. 1982. PMID: 7201972 No abstract available.

8

Expression of the fragile-X in the "premutated"/"non-imprinted" state.

Bilas R, Wilhelm D, Schwinger E, Chudley AE, Fryns JP, Howard-Peebles PN, Schinzel A, Van Roy B, Webb T. Bilas R, et al. Among authors: schwinger e. Genet Couns. 1992;3(4):179-81. Genet Couns. 1992. PMID: 1361753

9

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: schwinger e. Clin Genet. 1984 Dec;26(6):549-54. doi: 10.1111/j.1399-0004.1984.tb01102.x. Clin Genet. 1984. PMID: 6499266

10

[Puncture of the chorionic villi. Technic--experiences--risks].

Froster-Iskenius U, Klink F, Grzejszczyk G, Sömmer F, Schwinger E, Oberheuser F. Froster-Iskenius U, et al. Among authors: schwinger e. Zentralbl Gynakol. 1988;110(3):146-57. Zentralbl Gynakol. 1988. PMID: 3364066 German.

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