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Volumn 121 A, Issue 2, 2003, Pages 177-179
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Primary pulmonary dysgenesis in velocardiofacial syndrome: A second patient [2]
a
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Author keywords
[No Author keywords available]
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Indexed keywords
CASE REPORT;
CHROMOSOME 22;
CHROMOSOME DELETION;
CLINICAL FEATURE;
COMPUTER ASSISTED TOMOGRAPHY;
CONDUCTION DEAFNESS;
DIFFERENTIAL DIAGNOSIS;
EAR MALFORMATION;
ECHOCARDIOGRAPHY;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENE LOCUS;
HUMAN;
LETTER;
LUNG MALFORMATION;
MANDIBLE HYPOPLASIA;
NEURAL CREST;
PHYSICAL EXAMINATION;
PRESCHOOL CHILD;
PRIMARY PULMONARY DYSGENESIS;
PRIORITY JOURNAL;
SYNDROME DELINEATION;
VELOCARDIOFACIAL SYNDROME;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 22;
CRANIOFACIAL ABNORMALITIES;
DIGEORGE SYNDROME;
FEMALE;
HEART DEFECTS, CONGENITAL;
HUMANS;
IMMUNOLOGIC DEFICIENCY SYNDROMES;
INFANT;
LUNG;
LUNG DISEASES;
PULMONARY ARTERY;
SYNDROME;
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EID: 0042193653
PISSN: 15524825
EISSN: None
Source Type: Journal
DOI: None Document Type: Letter |
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Times cited : (16)
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References (5)
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