Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome) [2]

American Journal of Medical Genetics

Volumn 121 A, Issue 3, 2003, Pages 286-288

  Digilio, Maria Cristina ^a   Giannotti, Aldo ^a   Castro, Massimo ^a   Colistro, Franco ^a   Ferretti, Francesca ^a   Marino, Bruno ^b   Dallapiccola, Bruno ^b  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; CELIAC DISEASE; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CLINICAL FEATURE; DIETARY INTAKE; DIGEORGE SYNDROME; FEEDING BEHAVIOR; GASTROINTESTINAL SYMPTOM; GENE DELETION; GROWTH DISORDER; HUMAN; LETTER; PREVALENCE; PRIORITY JOURNAL; SCREENING; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CELIAC DISEASE; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FACE; FEMALE; HUMANS; MALE; PHENOTYPE; VELOPHARYNGEAL INSUFFICIENCY;

EID: 0042695819     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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