TY  - GEN
AU  - Steichen-Gersdorf,Elisabeth
AU  - Griesmaier,Elke
AU  - Pientka,Friederike K
AU  - Kotzot,Dieter
AU  - Kutsche,Kerstin
TI  - A severe form of the X-linked microphthalmia with linear skin defects syndrome in a female newborn
SN  - 1473-5717
PY  - 2010///0526
KW  - Abnormalities, Multiple
KW  - pathology
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, X
KW  - genetics
KW  - Female
KW  - Genes, X-Linked
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Microphthalmos
KW  - complications
KW  - Pregnancy
KW  - Skin Abnormalities
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1097/MCD.0b013e32833593b7
ER  -