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Volumn 37, Issue 9, 2000, Pages 701-704
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Interstitial deletion of chromosome 17 (del(17)(q22q23.3)) confirms a link with oesophageal atresia [2]
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Author keywords
[No Author keywords available]
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Indexed keywords
ANAMNESIS;
BLOOD CULTURE;
CASE REPORT;
CHILD;
CHROMOSOME 17;
CLINICAL FEATURE;
CONGENITAL MALFORMATION;
DISEASE COURSE;
ESOPHAGUS ATRESIA;
GENE LOCUS;
HUMAN;
INTERSTITIAL CHROMOSOME DELETION;
LETTER;
MALE;
PHYSICAL EXAMINATION;
PRIORITY JOURNAL;
TRACHEOESOPHAGEAL FISTULA;
CASE REPORT;
CHROMOSOME BANDING;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 17;
ESOPHAGEAL ATRESIA;
FATAL OUTCOME;
FEMALE;
HUMAN;
INFANT;
INFANT, NEWBORN;
KARYOTYPING;
MALE;
TRACHEOESOPHAGEAL FISTULA;
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EID: 0033828701
PISSN: 00222593
EISSN: None
Source Type: Journal
DOI: None Document Type: Letter |
Times cited : (51)
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References (12)
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