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Volumn 64, Issue 3, 2003, Pages 255-257
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Pure partial trisomy of 2q22-q23 secondary to a paternally inherited direct insertion: A rare duplication [2]
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Author keywords
[No Author keywords available]
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Indexed keywords
DNA;
ANTHROPOMETRY;
APGAR SCORE;
BIRTH WEIGHT;
CASE REPORT;
CHILDBIRTH;
CHROMOSOME 2Q;
CHROMOSOME 5;
CHROMOSOME ANALYSIS;
CHROMOSOME ARM;
CHROMOSOME BAND;
CHROMOSOME DUPLICATION;
CHROMOSOME INSERTION;
CLINICAL EXAMINATION;
CLINODACTYLY;
CYTOGENETICS;
DEVELOPMENTAL DISORDER;
DNA PROBE;
FACE MALFORMATION;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENE MAPPING;
HUMAN;
HYPOSPADIAS;
INFANT;
INHERITANCE;
KARYOTYPE 46,XY;
LETTER;
MALE;
MEDICAL LITERATURE;
PARTIAL TRISOMY;
PATIENT REFERRAL;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
ABNORMALITIES, MULTIPLE;
CHROMOSOME DISORDERS;
CHROMOSOMES, HUMAN, PAIR 2;
DEVELOPMENTAL DISABILITIES;
FACE;
FINGERS;
GENE DUPLICATION;
HEAD;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
INFANT, NEWBORN;
MALE;
MUTAGENESIS, INSERTIONAL;
TOES;
TRISOMY;
INSERTION SEQUENCES;
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EID: 0042914403
PISSN: 00099163
EISSN: None
Source Type: Journal
DOI: 10.1034/j.1399-0004.2003.00120.x Document Type: Letter |
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Times cited : (4)
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References (3)
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