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Volumn 39, Issue 1, 1996, Pages 51-53
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Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(q32;q22) in a male patient
a
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Author keywords
Autosomal translocation; Chromosome 13; Chromosome 9; Opitz C syndrome; Trigonocephaly
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Indexed keywords
ARTICLE;
AUTOSOMAL INHERITANCE;
CASE REPORT;
CHROMOSOME 9;
CLINICAL FEATURE;
CRANIOFACIAL MALFORMATION;
GROWTH RETARDATION;
HUMAN;
HUMAN CELL;
INFANT;
MALE;
MENTAL DEFICIENCY;
NEWBORN;
ORBIT DISEASE;
PRESCHOOL CHILD;
PTOSIS;
RECIPROCAL CHROMOSOME TRANSLOCATION;
SYMPTOM;
ABNORMALITIES, MULTIPLE;
BLEPHAROPTOSIS;
CHROMOSOMES, HUMAN, PAIR 13;
CHROMOSOMES, HUMAN, PAIR 9;
GROWTH DISORDERS;
HUMANS;
INFANT, NEWBORN;
MALE;
MENTAL RETARDATION;
ORBIT;
SYNDROME;
TRANSLOCATION, GENETIC;
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EID: 0029974634
PISSN: 00033995
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (7)
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References (0)
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