Szczerbal, Izabela Maria

Name

Szczerbal, Izabela

Scientific title

prof. dr hab.

ORCID

0000-0002-4238-0414

Faculty

Wydział Medycyny Weterynaryjnej i Nauk o Zwierzętach

Department

Katedra Genetyki i Podstaw Hodowli Zwierząt

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Cleft Lip and Palate in Four Full-Sib Puppies from a Single Litter of Staffordshire Bull Terrier Dogs: An Anatomical and Genetic Study

Nieprawidłowości chromosomów płci jako istotne przyczyny zaburzeń rozwoju płci kotów

SOX9 gene variants in 27 French Bulldogs with disorder of sex development (XX, SRY-negative): identification of first case of skeletal abnormalities associated with SOX9 triplication

Świnia - ważny gatunek modelowy w badaniach chorób genetycznych człowieka

XX/XY Chimerism in Internal Genitalia of a Virilized Heifer

Cytogenetic and molecular background of canine and feline disorders of sex development

Elevated serum concentration of anti‐Mullerian hormone and its association with SNP variants in the AMH gene in a tortoiseshell tomcat with a disorder of sex development (38,XX; SRY-negative)

Mutacje chromosomowe

Metody badania chromosomów

X monosomy in a British shorthair cat with skeletal abnormalities and behavioral problems

Lack of causative mutation in the AMH and AMHR2 genes in a cat (38,XY) with persistent Mullerian duct syndrome (PMDS)

Whole genome sequencing identifies a missense polymorphism in PADI6 associated with testicular/ovotesticular XX disorder of sex development in dogs

Testicular Disorder of Sex Development in a Mare With a Low Incidence of SRY‐Positive Cell Line in the Gonads

Non-mosaic X monosomy (77,X) in a female dog with signs of virilization

From cytogenetics to cytogenomics: a new era in the diagnosis of chromosomal abnormalities in domestic animals

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Cleft Lip and Palate in Four Full-Sib Puppies from a Single Litter of Staffordshire Bull Terrier Dogs: An Anatomical and Genetic Study

Nieprawidłowości chromosomów płci jako istotne przyczyny zaburzeń rozwoju płci kotów

SOX9 gene variants in 27 French Bulldogs with disorder of sex development (XX, SRY-negative): identification of first case of skeletal abnormalities associated with SOX9 triplication

Świnia - ważny gatunek modelowy w badaniach chorób genetycznych człowieka

XX/XY Chimerism in Internal Genitalia of a Virilized Heifer

Cytogenetic and molecular background of canine and feline disorders of sex development

Elevated serum concentration of anti‐Mullerian hormone and its association with SNP variants in the AMH gene in a tortoiseshell tomcat with a disorder of sex development (38,XX; SRY-negative)

Mutacje chromosomowe

Metody badania chromosomów

X monosomy in a British shorthair cat with skeletal abnormalities and behavioral problems

Lack of causative mutation in the AMH and AMHR2 genes in a cat (38,XY) with persistent Mullerian duct syndrome (PMDS)

Whole genome sequencing identifies a missense polymorphism in PADI6 associated with testicular/ovotesticular XX disorder of sex development in dogs

Testicular Disorder of Sex Development in a Mare With a Low Incidence of SRY‐Positive Cell Line in the Gonads

Non-mosaic X monosomy (77,X) in a female dog with signs of virilization

From cytogenetics to cytogenomics: a new era in the diagnosis of chromosomal abnormalities in domestic animals