TY  - GEN
AU  - Van Opstal,D
AU  - Eussen,H J
AU  - Van Hemel,J O
AU  - Sachs,E S
TI  - Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis
SN  - 0197-3851
PY  - 1994///0209
KW  - Adult
KW  - Amniocentesis
KW  - Chromosome Aberrations
KW  - diagnosis
KW  - Chromosome Banding
KW  - Chromosome Disorders
KW  - Chromosomes, Human, Pair 11
KW  - Chromosomes, Human, Pair 15
KW  - Chromosomes, Human, Pair 18
KW  - DNA Probes
KW  - Dandy-Walker Syndrome
KW  - Female
KW  - Fetal Diseases
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - methods
KW  - Infant, Newborn
KW  - Karyotyping
KW  - Pregnancy
KW  - Pregnancy Trimester, Second
KW  - Pregnancy Trimester, Third
KW  - Prenatal Diagnosis
KW  - Translocation, Genetic
KW  - Trisomy
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/pd.1970130906
ER  -