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Person

Christina Evers (1978-)

Ärztin

Name	Christina Evers
Time	1978- (Date of birth and death)
Place	Geldern (Geburtsort) Deutschland
Academic degree	Dr. med.
Profession	Ärztin (characteristic profession)
Variant	Christina M. Evers Christina Maria Evers
Related	Universität Heidelberg. Institut für Humangenetik
Further information	Diss. Fachbereich Medizin
Record type	Person
GND-Identifier	13388340X
Record ID	13388340X
Involved in show all Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis Women at familial risk of breast cancer electing for prophylactic mastectomy: frequencies, procedures, and decision-making characteristics Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of Literature DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome Impact of clinical exomes in neurodevelopmental and neurometabolic disorders Adherence to the breast cancer surveillance program for women at risk for familial breast and ovarian cancer versus overscreening: a monocenter study in Germany Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy Phenotypic and molecular insights into CASK-related disorders in males SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract Charakterisierung der Oncostatin-M-vermittelten STAT5-Aktivierung : Beitrag des Rezeptorkomplexes und der Januskinasen Charakterisierung der Oncostatin-M-vermittelten STAT5-Aktivierung : Beitrag des Rezeptorkomplexes und der Januskinasen

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Christina Evers (1978-)

Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis

Women at familial risk of breast cancer electing for prophylactic mastectomy: frequencies, procedures, and decision-making characteristics

Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of Literature

DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome

Impact of clinical exomes in neurodevelopmental and neurometabolic disorders

Adherence to the breast cancer surveillance program for women at risk for familial breast and ovarian cancer versus overscreening: a monocenter study in Germany

Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy

Phenotypic and molecular insights into CASK-related disorders in males

SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract

Charakterisierung der Oncostatin-M-vermittelten STAT5-Aktivierung : Beitrag des Rezeptorkomplexes und der Januskinasen

Charakterisierung der Oncostatin-M-vermittelten STAT5-Aktivierung : Beitrag des Rezeptorkomplexes und der Januskinasen