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المؤلفون: rer. nat. R.-D. Wegner, M. Stumm
المصدر: Medizinische Genetik. 23:457-462
مصطلحات موضوعية: Gynecology, medicine.medical_specialty, business.industry, Genetics, medicine, business, Genetics (clinical)
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المؤلفون: F. Nürnberger, R.-D. Wegner
المصدر: Andrologia. 15:253-258
مصطلحات موضوعية: Adult, Male, Endocrinology, Karyotyping, Urology, H-Y Antigen, Humans, General Medicine, Infertility, Male, Sex Chromosome Aberrations, Chromosome Banding
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المؤلفون: A. Schmidt, Albert Schinzel, H. Zankl, A. Wirtz, H. Veenema, R.-D. Wegner, Merve Zankl, E. Kab, Ursula Froster-Iskenius, Eberhard Schwinger, U. Langenbeck, A. Rodewald, Peter Steinbach
المساهمون: University of Zurich, Rodewald, A
المصدر: Clinical Genetics. 30:1-13
مصطلحات موضوعية: Adult, Male, 2716 Genetics (clinical), X Chromosome, Adolescent, 10039 Institute of Medical Genetics, Genetic Linkage, Dermatoglyphic patterns, 610 Medicine & health, Papillary ridges, Biology, 1311 Genetics, Intellectual Disability, Genetics, medicine, Humans, Dermatoglyphics, Child, Sex Chromosome Aberrations, Genetics (clinical), Genetic Carrier Screening, Chromosomal fragile site, Anatomy, medicine.disease, body regions, Fragile X syndrome, Male patient, Child, Preschool, Fragile X Syndrome, Clinical diagnosis, 570 Life sciences, biology, Female
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المؤلفون: Ivo Henrichs, R. D. Wegner, Traute M. Schroeder-Kurth, Hans Joenje
المصدر: Clinical Genetics. 50:479-482
مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Turkey, Diepoxybutane, Biology, Fingers, Consanguinity, chemistry.chemical_compound, Fatal Outcome, Fanconi anemia, hemic and lymphatic diseases, Chromosome instability, Hypotelorism, Genetics, medicine, Chromosomes, Human, Humans, Lymphocytes, Syndactyly, Genetics (clinical), Cell Line, Transformed, Genetic Complementation Test, Brachydactyly, Infant, Newborn, medicine.disease, Hypoplasia, Fanconi Anemia, Phenotype, chemistry, Brachycephaly
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المؤلفون: Regina Bendix-Waltes, Thilo Dörk, R. D. Wegner, Markus Stumm
المصدر: American Journal of Medical Genetics Part A. :272-277
مصطلحات موضوعية: Genetics, Mutation, Ataxia, Wild type, Biology, medicine.disease_cause, medicine.disease, Compound heterozygosity, Nibrin, Chromosome instability, Ataxia-telangiectasia, medicine, Cancer research, Missense mutation, medicine.symptom, Genetics (clinical)
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المؤلفون: Susanne Sohl, Michael Entezami, Denise Horn, R. D. Wegner, Ute Knoll, Rolf Becker
المصدر: American Journal of Medical Genetics. :85-88
مصطلحات موضوعية: Adult, Heart Defects, Congenital, Male, Pathology, medicine.medical_specialty, Foot Deformities, Congenital, Aneuploidy, Trisomy, Prenatal diagnosis, Biology, Pregnancy, Prenatal Diagnosis, medicine, Humans, Genetics (clinical), Genetics, Fetus, Amniotic fluid cells, Mosaicism, Infant, Newborn, Chromosome, medicine.disease, Phenotype, Pregnancy Trimester, Second, Gestation, Chromosomes, Human, Pair 6, Female, Hand Deformities, Congenital
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4505aac35e534741782eac110c3a11a3
https://doi.org/10.1002/ajmg.a.20407 -
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المؤلفون: Rolf Becker, R. D. Wegner, Gundula Thiel, Rainer Bollmann, Ines Schulzke, H. Körner, C. Tennstedt, Christiane Bommer, Katarina Lehmann, Maik Urban
المصدر: American Journal of Medical Genetics. 108:97-104
مصطلحات موضوعية: Genetics, Monosomy, Pediatrics, medicine.medical_specialty, Autosome, medicine.diagnostic_test, Ring chromosome, Prenatal diagnosis, Biology, medicine.disease, Short stature, Hydrocephalus, Aqueductal stenosis, medicine, Amniocentesis, medicine.symptom, Genetics (clinical)
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المؤلفون: Heidemarie Neitzel, Rudolf Kaden, Peter Vogt, Gerd Scherer, R. D. Wegner, Klaus Grossgebauer, Karl Sperling
المصدر: International Journal of Human Genetics. 1:113-116
مصطلحات موضوعية: Genetics, Infertility, urogenital system, fungi, Karyotype, Biology, Y chromosome, medicine.disease, Sperm, Andrology, Prophase, Polyploid, Meiosis, medicine, Germ, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::4e48ca0c7d0eda5d2807b15417b85242
https://doi.org/10.1080/09723757.2001.11885744 -
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المؤلفون: M. Guschmann, R. D. Wegner, Michael Entezami, Rolf Becker, B. Stiemer, L. Schmitz
المصدر: Ultrasound in Obstetrics and Gynecology. 17:263-267
مصطلحات موضوعية: medicine.medical_specialty, Pregnancy, Fetus, Radiological and Ultrasound Technology, business.industry, Obstetrics and Gynecology, Prenatal diagnosis, Autopsy, General Medicine, medicine.disease, Surgery, medicine.anatomical_structure, Reproductive Medicine, Double outlet right ventricle, Pulmonary valve, medicine, Gestation, Radiology, Nuclear Medicine and imaging, business, Tetralogy of Fallot
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المؤلفون: GR Evans, H Joenje, Fré Arwert, Martin Digweed, Cigdem Altay, R. D. Wegner, Neil V. Morgan, André Reis, Kathrin Saar, Christopher G. Mathew, Quinten Waisfisz, J. de Winter, Peter A. J. Leegwater, Kenshi Komatsu, Jan C. Pronk
المساهمون: Clinical genetics, Clinical chemistry, Çocuk Sağlığı ve Hastalıkları
المصدر: American journal of human genetics, 64(5), 1400-1405. Cell Press
Waisfisz, Q, Altay, C, Leegwater, PA, de Winter, JP, Komatsu, K, Evans, GR, Wegner, RD, Reis, A, Joenje, H, Arwert, F, Mathew, CG, Pronk, JC, Saar, K, Morgan, NV & Digweed, M 1999, ' The Fanconi anemia group E gene, FANCE, maps to chromosome 6p ', American journal of human genetics, vol. 64, no. 5, pp. 1400-1405 . https://doi.org/10.1086/302385مصطلحات موضوعية: Genetic Markers, Male, Fanconi anemia, complementation group C, Locus (genetics), Complementation analysis, Biology, FANCE, Gene mapping, Fanconi anemia, Homozygosity mapping, Genetics, medicine, Humans, Genetics(clinical), Cell fusion, Genetics (clinical), Genetics & Heredity, Genetic Complementation Test, Chromosome Mapping, Chromosome Fragility, medicine.disease, Genetic marker, FANCE Gene, Chromosomes, Human, Pair 6, Female, Chromosome 6p21-22, Research Article
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