Palavra-chave: CYTOGENETICS

ABERRAÇÃO CROMOSSÔMICA NOR HIPERTELORISMO FENDAS LABIOPALATAIS COPY NUMBER VARIANTS SEX CHROMOSOMES ANOMALIAS CRANIOFACIAIS CHRONIC EOSINOPHILIC LEUKAEMIA FANCA ANURA FENDAS OROFACIAIS PHYSALAMEUS LOW-PASS WHOLE GENOME SEQUENCING HETEROCHROMATIN SNP-ARRAY DEFEITOS CONGÊNITOS FLUORESCENCE IN SITU HIBRIDIZATYION MOLECULAR CYTOGENETICS GENÉTICA MOLECULAR RETT SYNDROME LOW-PASS WHOLE GENOME CÁPSULA NASAL ARRAY-CGH FRAGILE X SYNDROME SCYTHROPHRYS STRUCTURAL VARIANTS KARYOTYPE SCUTHROPHRYS DISPLASIA FRONTONASAL NEXT GENERATION SEQUENCING (NGS) DES TEST TRANSPLANTATION WES GENÉTICA HUMANA E MÉDICA MOLECULAR STUDIES EDALORHINA POLYMORPHISM PERICENTRIC INVERSION PROGNOSIS PHYSALAEMUS CARDIOPATIA CHROMOSOMAL ABNORMALITIES PLASMA CELL LEUKEMIA PARATELMATOBIUS MEIOTIC RINGS LEPTODACTYLIDAE AGH COPY NUMBER VARIATIONS CROMOSSOMO 18 BORTEZOMIB CHROMOSOMAL MICROARRAY ANALYSIS TRANSLOCATION POSTNATAL DIAGNOSIS DEFEITOS DE LINHA MÉDIA FACIAL COM HIPERTELORISMO MYELOMA FANCONI ANAEMIA CNV LEPTODACTYLDIAE CITOGENÉTICA FANCC