Rehder H - Search Results

1

Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): further delineation of trisomies 1q.

Bartsch C, Aslan M, Köhler J, Miny P, Horst J, Holzgreve W, Rehder H, Fritz B. Bartsch C, et al. Among authors: rehder h. Fetal Diagn Ther. 2001 Sep-Oct;16(5):265-73. doi: 10.1159/000053926. Fetal Diagn Ther. 2001. PMID: 11509847

2

[Diagnosis of fetal virus infections by in situ hybridization].

Mehraein Y, Rehder H, Draeger HG, Froster-Iskenius UG, Schwinger E, Holzgreve W. Mehraein Y, et al. Among authors: rehder h. Geburtshilfe Frauenheilkd. 1991 Dec;51(12):984-9. doi: 10.1055/s-2008-1026249. Geburtshilfe Frauenheilkd. 1991. PMID: 1665465 German.

3

Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and newborn.

Ramsing M, Rehder H, Holzgreve W, Meinecke P, Lenz W. Ramsing M, et al. Among authors: rehder h. Clin Genet. 1990 Feb;37(2):84-96. doi: 10.1111/j.1399-0004.1990.tb03484.x. Clin Genet. 1990. PMID: 2155726

4

Cardiac defects in chromosomally abnormal human embryos of 10-14 weeks' gestation.

Coerdt W, Rehder H, Gebauer HJ, Holzgreve W, Klink F, Miny P, Schulze B. Coerdt W, et al. Among authors: rehder h. Prenat Diagn. 1988 Nov;8(9):647-59. doi: 10.1002/pd.1970080904. Prenat Diagn. 1988. PMID: 2974956

5

[Ultrasound findings as a sign of fetal triploidy].

Holzgreve W, Miny P, Holzgreve A, Rehder H. Holzgreve W, et al. Among authors: rehder h. Ultraschall Med. 1986 Aug;7(4):169-71. doi: 10.1055/s-2007-1011939. Ultraschall Med. 1986. PMID: 3538408 German.

6

Bilateral renal agenesis with Potter phenotype, cleft palate, anomalies of the cardiovascular system, skeletal anomalies including hexadactyly and bifid metacarpal. A new syndrome?

Holzgreve W, Wagner H, Rehder H. Holzgreve W, et al. Among authors: rehder h. Am J Med Genet. 1984 May;18(1):177-82. doi: 10.1002/ajmg.1320180122. Am J Med Genet. 1984. PMID: 6741992 No abstract available.

7

Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally.

Miny P, Koppers B, Dworniczak B, Bogdanova N, Holzgreve W, Tercanli S, Basaran S, Rehder H, Exeler R, Horst J. Miny P, et al. Among authors: rehder h. Am J Med Genet. 1995 May 22;57(1):102-6. doi: 10.1002/ajmg.1320570121. Am J Med Genet. 1995. PMID: 7645587

8

Extreme hypotrophy of the lower body pole, extensive hypoplasia of the spinal column and multiple anomalies of abdominal organs: a maximal variant of the caudal regression sequence?

Rossi R, Holzgreve W, Rehder H. Rossi R, et al. Among authors: rehder h. Clin Dysmorphol. 1995 Jan;4(1):87-92. doi: 10.1097/00019605-199501000-00014. Clin Dysmorphol. 1995. PMID: 7735512

9

[Possibilities for false-negative findings in trisomy 21 screening with FISH].

Fritz B, Van Oorschot B, Latta E, Rehder H. Fritz B, et al. Among authors: rehder h. Z Geburtshilfe Neonatol. 1996 Sep-Oct;200(5):191-8. Z Geburtshilfe Neonatol. 1996. PMID: 9035829 German.

10

Microdeletion 22q11 in complex cardiovascular malformations.

Mehraein Y, Wippermann CF, Michel-Behnke I, Nhan Ngo TK, Hillig U, Giersberg M, Aulepp U, Barth H, Fritz B, Rehder H. Mehraein Y, et al. Among authors: rehder h. Hum Genet. 1997 Apr;99(4):433-42. doi: 10.1007/s004390050385. Hum Genet. 1997. PMID: 9099830

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