R-D Wegner - JoVE Visualize

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Der Urologe. Ausg. A|July 1, 1994

[Mixed gonadal dysgenesis--a rare cause of primary infertility. Report of 2 cases and review of the literature]H E Wegner, A Ferszt, R D Wegner, et al.

Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1991

Frequency of trisomy 21 in Germany before and after the Chernobyl accidentK Sperling, J Pelz, R D Wegner, et al.

Padiatrie Und Padologie|January 1, 1986

Cri du chat-syndrome in combination with partial trisomy 9 pJ Sigmund, H Frisch, P Heinz-Erian, et al.

Cytogenetics and Cell Genetics|August 31, 2001

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnosticsH Tönnies, M Stumm, R D Wegner, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 20, 2001

Prenatal diagnosis of familial absent pulmonary valve syndrome: case report and review of the literatureR Becker, L Schmitz, M Guschmann, et al.

Cytogenetics and Cell Genetics|July 4, 2001

High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndromeM Stumm, S Neubauer, S Keindorff, et al.

Prenatal Diagnosis|August 1, 1996

Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term cultureR D Wegner, E Schröck, M Obladen, et al.

BMJ (Clinical Research Ed.)|July 16, 1994

Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?K Sperling, J Pelz, R D Wegner, et al.

Human Genetics|February 1, 1991

Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenitaM Stuhrmann, H Heilbronner, A Reis, et al.

Clinical Genetics|March 29, 2000

Clinical variability of Larsen syndrome: diagnosis in a father after sonographic detection of a severely affected fetusR Becker, R D Wegner, J Kunze, et al.

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Showing results (21-30 of 58) with videos related to

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Der Urologe. Ausg. A|July 1, 1994

[Mixed gonadal dysgenesis--a rare cause of primary infertility. Report of 2 cases and review of the literature]H E Wegner, A Ferszt, R D Wegner, et al.

Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1991

Frequency of trisomy 21 in Germany before and after the Chernobyl accidentK Sperling, J Pelz, R D Wegner, et al.

Padiatrie Und Padologie|January 1, 1986

Cri du chat-syndrome in combination with partial trisomy 9 pJ Sigmund, H Frisch, P Heinz-Erian, et al.

Cytogenetics and Cell Genetics|August 31, 2001

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnosticsH Tönnies, M Stumm, R D Wegner, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 20, 2001

Prenatal diagnosis of familial absent pulmonary valve syndrome: case report and review of the literatureR Becker, L Schmitz, M Guschmann, et al.

Cytogenetics and Cell Genetics|July 4, 2001

High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndromeM Stumm, S Neubauer, S Keindorff, et al.

Prenatal Diagnosis|August 1, 1996

Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term cultureR D Wegner, E Schröck, M Obladen, et al.

BMJ (Clinical Research Ed.)|July 16, 1994

Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?K Sperling, J Pelz, R D Wegner, et al.

Human Genetics|February 1, 1991

Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenitaM Stuhrmann, H Heilbronner, A Reis, et al.

Clinical Genetics|March 29, 2000

Clinical variability of Larsen syndrome: diagnosis in a father after sonographic detection of a severely affected fetusR Becker, R D Wegner, J Kunze, et al.

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