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Plant Physiology
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April 24, 2010
An autoinhibitory domain confers redox regulation to maize glycerate kinase
Oliver Bartsch, Stefan Mikkat, Martin Hagemann, et al.
Ophthalmic Genetics
|
December 29, 2007
Two novel deletions (array CGH findings) in pigment dispersion syndrome
Ruth Mikelsaar, Harras Molder, Oliver Bartsch, et al.
American Journal of Medical Genetics. Part A
|
August 1, 2012
Case report: Noonan syndrome with multiple giant cell lesions and review of the literature
Julia Karbach, Wiltrud Coerdt, Wilfried Wagner, et al.
American Journal of Medical Genetics
|
March 29, 2002
Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 --> qter, and trisomy 8q24.3 --> qter
Katrin Ounap, Oliver Bartsch, Oivi Uibo, et al.
American Journal of Medical Genetics. Part A
|
April 13, 2011
Familial ring (18) mosaicism in a 23-year-old young adult with 46,XY,r(18) (::p11→q21::)/46,XY karyotype, intellectual disability, motor retardation and single maxillary incisor and in his phenotypically normal mother, karyotype 47,XX,+r(18)(::p11→q21::)/46,XX
Sevim Balci, Celal Tümer, Ciğdem Karaca, et al.
American Journal of Medical Genetics. Part A
|
February 20, 2020
A female with X-linked Nephrogenic diabetes insipidus in a family with inherited central diabetes Insipidus: Case report and review of the literature
Can Ding, Rolf Beetz, Gabriele Rittner, et al.
American Journal of Medical Genetics
|
October 31, 2002
Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies
Cristina Skrypnyk, Timm O Goecke, Frank Majewski, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2010
Rubinstein-Taybi syndrome in first cousins with different de novo mutations
Sevim Balci, Mehmet Ali Ergün, Stanislav Lechno, et al.
Hormones and Behavior
|
February 15, 2005
Androstadienone odor thresholds in adolescents
Thomas Hummel, Franziska Krone, Johan N Lundström, et al.
American Journal of Medical Genetics. Part A
|
November 4, 2004
Two sisters with Silver-Russell phenotype
Katrin Ounap, Tiia Reimand, Marja-Liis Mägi, et al.
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of 12
Search research articles
Search
Showing results (11-20 of 118) with videos related to
Sort By:
Page
of 12
Plant Physiology
|
April 24, 2010
An autoinhibitory domain confers redox regulation to maize glycerate kinase
Oliver Bartsch, Stefan Mikkat, Martin Hagemann, et al.
Ophthalmic Genetics
|
December 29, 2007
Two novel deletions (array CGH findings) in pigment dispersion syndrome
Ruth Mikelsaar, Harras Molder, Oliver Bartsch, et al.
American Journal of Medical Genetics. Part A
|
August 1, 2012
Case report: Noonan syndrome with multiple giant cell lesions and review of the literature
Julia Karbach, Wiltrud Coerdt, Wilfried Wagner, et al.
American Journal of Medical Genetics
|
March 29, 2002
Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 --> qter, and trisomy 8q24.3 --> qter
Katrin Ounap, Oliver Bartsch, Oivi Uibo, et al.
American Journal of Medical Genetics. Part A
|
April 13, 2011
Familial ring (18) mosaicism in a 23-year-old young adult with 46,XY,r(18) (::p11→q21::)/46,XY karyotype, intellectual disability, motor retardation and single maxillary incisor and in his phenotypically normal mother, karyotype 47,XX,+r(18)(::p11→q21::)/46,XX
Sevim Balci, Celal Tümer, Ciğdem Karaca, et al.
American Journal of Medical Genetics. Part A
|
February 20, 2020
A female with X-linked Nephrogenic diabetes insipidus in a family with inherited central diabetes Insipidus: Case report and review of the literature
Can Ding, Rolf Beetz, Gabriele Rittner, et al.
American Journal of Medical Genetics
|
October 31, 2002
Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies
Cristina Skrypnyk, Timm O Goecke, Frank Majewski, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2010
Rubinstein-Taybi syndrome in first cousins with different de novo mutations
Sevim Balci, Mehmet Ali Ergün, Stanislav Lechno, et al.
Hormones and Behavior
|
February 15, 2005
Androstadienone odor thresholds in adolescents
Thomas Hummel, Franziska Krone, Johan N Lundström, et al.
American Journal of Medical Genetics. Part A
|
November 4, 2004
Two sisters with Silver-Russell phenotype
Katrin Ounap, Tiia Reimand, Marja-Liis Mägi, et al.
Page
of 12