Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion

American Journal of Medical Genetics, Part A

Volumn 146, Issue 9, 2008, Pages 1134-1141

  Fernández, Luis ^a,b   Lapunzina, Pablo ^a,b   Pajares, Isidora López ^a,b   Palomares, María ^a,b   Martínez, Isabel ^a,b   Fernández, Blanca ^a,b   Quero, José ^a   García Guereta, Luis ^a   García Alix, Alfredo ^a   Burgueros, Margarita ^a   Galán Gómez, Enrique ^c   Carbonell Pérez, José María ^c   Pérez Granero, Ángeles ^d   Torres Juan, Laura ^d   Heine Suñer, Damià ^d   Rosell, Jordi ^d   Delicado, Alicia ^a,b  

^a HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^c HOSPITAL INFANTA CRISTINA   (Spain)

^d HOSPITAL UNIVERSITARIO SON ESPASES   (Spain)

Author keywords

22q11.2 deletion syndrome; DiGeorge anomaly; Unrelated chromosomal anomalies; Velocardiofacial syndrome

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CLINICAL PROTOCOL; CONTROLLED STUDY; CORRELATION ANALYSIS; CYTOGENETICS; DIGEORGE SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; SEX CHROMOSOME ABERRATION; VELOCARDIOFACIAL SYNDROME;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CONGENITAL ABNORMALITIES; DIGEORGE SYNDROME; FEMALE; GENETIC SCREENING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PHENOTYPE; SPAIN; SYNDROME;

EID: 43049115700     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32256     Document Type: Article

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