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Fortschritte Der Kieferorthopadie
|
June 1, 1983
[Familial tooth position anomalies in the Orangutang. Orthodontic, cytogenetic and anthropological studies]
G Schwanitz, K Keft, A Fleischer-Peters, et al.
Clinical Genetics
|
July 28, 1999
Characterisation, phenotypic manifestations and X-inactivation pattern in 14 patients with X-autosome translocations
B Kalz-Füller, E Sleegers, G Schwanitz, et al.
Klinische Padiatrie
|
May 1, 1973
[Ring chromosome D13-case history and survey (author's transl)]
U Zink, R Rix, K P Grosse, et al.
Annales De Genetique
|
January 9, 1999
A case of de novo translocation 16;21: trisomy 16q phenotype and origin of the aberration
T Eggermann, I Kolin-Gerresheim, F Gerresheim, et al.
Annales De Genetique
|
January 1, 1993
Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling
T Eggermann, M M Nöthen, P Propping, et al.
Bericht Uber Die Zusammenkunft. Deutsche Ophthalmologische Gesellschaft
|
January 1, 1978
[A new chromosome aberration with bilateral microphthalmos and right-sided orbital cyst]
U Mayer, G Schwanitz, K P Grosse, et al.
Humangenetik
|
September 10, 1975
Partial trisomy 10p
K P Grosse, G Schwanitz, H Singer, et al.
Annales De Genetique
|
September 1, 1978
[Partial trisomy 2p due to a familial translocation 2/6. Cytogenetic and clinical case with special reference to ophthalmologic changes]
U Mayer, G Schwanitz, K P Grosse, et al.
Annales De Genetique
|
January 1, 1988
Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17
G Schwanitz, K Zerres, M Niesen, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1971
[Mosaic Down's syndrome]
K P Grosse, G Grosse, G Schwanitz, et al.
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of 13
Search research articles
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Showing results (51-60 of 123) with videos related to
Sort By:
Page
of 13
Fortschritte Der Kieferorthopadie
|
June 1, 1983
[Familial tooth position anomalies in the Orangutang. Orthodontic, cytogenetic and anthropological studies]
G Schwanitz, K Keft, A Fleischer-Peters, et al.
Clinical Genetics
|
July 28, 1999
Characterisation, phenotypic manifestations and X-inactivation pattern in 14 patients with X-autosome translocations
B Kalz-Füller, E Sleegers, G Schwanitz, et al.
Klinische Padiatrie
|
May 1, 1973
[Ring chromosome D13-case history and survey (author's transl)]
U Zink, R Rix, K P Grosse, et al.
Annales De Genetique
|
January 9, 1999
A case of de novo translocation 16;21: trisomy 16q phenotype and origin of the aberration
T Eggermann, I Kolin-Gerresheim, F Gerresheim, et al.
Annales De Genetique
|
January 1, 1993
Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling
T Eggermann, M M Nöthen, P Propping, et al.
Bericht Uber Die Zusammenkunft. Deutsche Ophthalmologische Gesellschaft
|
January 1, 1978
[A new chromosome aberration with bilateral microphthalmos and right-sided orbital cyst]
U Mayer, G Schwanitz, K P Grosse, et al.
Humangenetik
|
September 10, 1975
Partial trisomy 10p
K P Grosse, G Schwanitz, H Singer, et al.
Annales De Genetique
|
September 1, 1978
[Partial trisomy 2p due to a familial translocation 2/6. Cytogenetic and clinical case with special reference to ophthalmologic changes]
U Mayer, G Schwanitz, K P Grosse, et al.
Annales De Genetique
|
January 1, 1988
Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17
G Schwanitz, K Zerres, M Niesen, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1971
[Mosaic Down's syndrome]
K P Grosse, G Grosse, G Schwanitz, et al.
Page
of 13