Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion.
Courtens, W
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion. [electronic resource] - Human genetics Oct 1998 - 497-505 p. digital
Publication Type: Case Reports; Journal Article
0340-6717
10.1007/s004390050857 doi
Chromosome Deletion
Chromosome Inversion
Chromosomes, Human, Pair 18
Humans
In Situ Hybridization, Fluorescence
Infant, Newborn
Male
Microsatellite Repeats
Mothers
Noonan Syndrome--genetics
Phenotype
Twins, Monozygotic--genetics
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion. [electronic resource] - Human genetics Oct 1998 - 497-505 p. digital
Publication Type: Case Reports; Journal Article
0340-6717
10.1007/s004390050857 doi
Chromosome Deletion
Chromosome Inversion
Chromosomes, Human, Pair 18
Humans
In Situ Hybridization, Fluorescence
Infant, Newborn
Male
Microsatellite Repeats
Mothers
Noonan Syndrome--genetics
Phenotype
Twins, Monozygotic--genetics