Phenotypic and cytogenetic spectrum of 9p trisomy

Genetic Counseling

Volumn 18, Issue 1, 2007, Pages 29-48

  Temtamy, Samia A ^a   Kamel, A K ^a   Ismail, S ^a   Helmy, N A ^a   Aglan, M S ^a   El Gammal, M ^a   El Ruby, M ^a   Mohamed, A M ^a  

^a NATIONAL RESEARCH CENTRE   (Egypt)

Author keywords

Coffin Siris syndrome; Phenotype karyotype correlations; Trisomy 9p

Indexed keywords

AGENESIS; ARTICLE; BRAIN MALFORMATION; CHILD; CHROMOSOME 9P; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME DUPLICATION; CHROMOSOME STRUCTURE; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CLINICAL FEATURE; COFFIN SIRIS SYNDROME; DANDY WALKER SYNDROME; FEMALE; GENE LOCATION; GENETIC ASSOCIATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPOPLASIA; MALE; MENTAL DEFICIENCY; NUCLEAR MAGNETIC RESONANCE IMAGING; PARTIAL TRISOMY 9; RATING SCALE;

ABNORMALITIES, MULTIPLE; CHILD; CHILD, PRESCHOOL; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 9; CYTOGENETIC ANALYSIS; FEMALE; GENOTYPE; HUMANS; INFANT; KARYOTYPING; MALE; PHENOTYPE; SYNDROME; TRISOMY;

EID: 34247520468     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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