Trisomy 12p and monosomy 4p: phenotype-genotype correlation.

Genetic testing and molecular biomarkers

Volumn 13, Issue 2, 2009, Pages 199-204

  Benussi, Daniela Gambel ^a   Costa, Paola ^a   Zollino, Marcella ^a   Murdolo, Marina ^a   Petix, Vincenzo ^a   Carrozzi, Marco ^a   Pecile, Vanna ^a  

^a INSTITUTE FOR MATERNAL AND CHILD HEALTH IRCCS BURLO GAROFOLO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CASE REPORT; CHROMOSOME 12; CHROMOSOME 4; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; EPILEPSY; FACIES; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE TRANSLOCATION; GENETICS; GENOTYPE; HUMAN; KARYOTYPING; MENTAL DEFICIENCY; MOLECULAR PROBE; MUSCLE HYPOTONIA; PHENOTYPE; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; TRISOMY; WOLF HIRSCHHORN SYNDROME;

CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, ARTIFICIAL, BACTERIAL; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 4; EPILEPSY; FACIES; FEMALE; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MENTAL RETARDATION; MOLECULAR PROBES; MUSCLE HYPOTONIA; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; TRANSLOCATION, GENETIC; TRISOMY; WOLF-HIRSCHHORN SYNDROME;

EID: 67650067629     PISSN: None     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2008.0109     Document Type: Article

References (0)