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Cytogenetics and Cell Genetics
|
August 31, 2001
Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics
H 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 literature
R 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 syndrome
M 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 culture
R 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 congenita
M Stuhrmann, H Heilbronner, A Reis, et al.
BMJ (Clinical Research Ed.)
|
November 12, 1994
Fallout from Chernobyl. Authors stand by study that Chernobyl increased trisomy 21 in Berlin
K Sperling, J Pelz, R D Wegner, et al.
Clinical Genetics
|
March 29, 2000
Clinical variability of Larsen syndrome: diagnosis in a father after sonographic detection of a severely affected fetus
R Becker, R D Wegner, J Kunze, et al.
Human Genetics
|
October 1, 1993
Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephaly
N Tommerup, E Mortensen, M H Nielsen, et al.
Geburtshilfe Und Frauenheilkunde
|
August 1, 1989
[Experiences with transcervical chorionic villi biopsy in 274 studies]
G Karkut, R Becker, K Starzinski, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 67) with videos related to
Sort By:
Page
of 7
Cytogenetics and Cell Genetics
|
August 31, 2001
Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics
H 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 literature
R 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 syndrome
M 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 culture
R 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 congenita
M Stuhrmann, H Heilbronner, A Reis, et al.
BMJ (Clinical Research Ed.)
|
November 12, 1994
Fallout from Chernobyl. Authors stand by study that Chernobyl increased trisomy 21 in Berlin
K Sperling, J Pelz, R D Wegner, et al.
Clinical Genetics
|
March 29, 2000
Clinical variability of Larsen syndrome: diagnosis in a father after sonographic detection of a severely affected fetus
R Becker, R D Wegner, J Kunze, et al.
Human Genetics
|
October 1, 1993
Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephaly
N Tommerup, E Mortensen, M H Nielsen, et al.
Geburtshilfe Und Frauenheilkunde
|
August 1, 1989
[Experiences with transcervical chorionic villi biopsy in 274 studies]
G Karkut, R Becker, K Starzinski, et al.
Page
of 7