TY  - GEN
AU  - Courtens,W
AU  - Grossman,D
AU  - Van Roy,N
AU  - Messiaen,L
AU  - Vamos,E
AU  - Toppet,V
AU  - Haumont,D
AU  - Streydio,C
AU  - Jauch,A
AU  - Vermeesch,J R
AU  - Speleman,F
TI  - Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion
SN  - 0340-6717
PY  - 1998///1223
KW  - Chromosome Deletion
KW  - Chromosome Inversion
KW  - Chromosomes, Human, Pair 18
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant, Newborn
KW  - Male
KW  - Microsatellite Repeats
KW  - Mothers
KW  - Noonan Syndrome
KW  - genetics
KW  - Phenotype
KW  - Twins, Monozygotic
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1007/s004390050857
ER  -