Molecular Cytogenetics | |
Diagnosis of structural and numerical abnormalities in chromosomes, characterization of submicroscopic deletions and rearrangements, identification of unknown chromosome material. | |
![]() |
FISH for SMITH-MAGENIS Syndrome - |
![]() |
FISH for WOLF-HIRSCHHORN Syndrome - |
![]() |
FISH for CRI-DU-CHAT Syndrome - |
![]() |
FISH for DI GEORGE Syndrome - |
![]() |
FISH for KALLMANN (KAL) Syndrome - |
![]() |
FISH for MILLER DIEKER /LISSENCEPHALY Syndrome - |
![]() |
FISH for PRADER WILLI /ANGELMAN Syndrome - |
![]() |
FISH for WILLIAMS Syndrome - |
![]() |
FISH - interphase amniotic cells (13, 18, 21, X, Y) - |
![]() |
FISH - interphase amniotic cells (21 e X,Y) - |
![]() |
FISH with PAINTING Probes - |
![]() |
Sperm FISH - |