TY  - GEN
AU  - Wauters,J G
AU  - Bossuyt,P J
AU  - Roelen,L
AU  - van Roy,B
AU  - Dumon,J
TI  - Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion
SN  - 0009-9163
PY  - 1994///0324
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Abortion, Therapeutic
KW  - Chromosome Aberrations
KW  - Chromosome Disorders
KW  - Chromosome Inversion
KW  - Chromosomes, Human, Pair 6
KW  - Facial Bones
KW  - abnormalities
KW  - Female
KW  - Fetal Diseases
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant, Newborn
KW  - Intellectual Disability
KW  - genetics
KW  - Kidney
KW  - Male
KW  - Monosomy
KW  - Mosaicism
KW  - Pedigree
KW  - Pregnancy
KW  - Pregnancy Trimester, First
KW  - Pregnancy Trimester, Second
KW  - Pregnancy in Diabetics
KW  - Prenatal Diagnosis
KW  - Skull
KW  - Trisomy
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1111/j.1399-0004.1993.tb03894.x
ER  -