Renal malformations in deletion 22q11.2 patients [1]

American Journal of Medical Genetics, Part A

Volumn 140, Issue 14, 2006, Pages 1601-1602

  Kujat, Annegret ^a   Schulz, Marc D ^a   Strenge, Sibylle ^a   Froster, Ursula G ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CYTOGENETICS; DIGEORGE SYNDROME; EMBRYO DEVELOPMENT; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; KIDNEY DEVELOPMENT; KIDNEY MALFORMATION; LETTER; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FACIAL BONES; HEART DEFECTS, CONGENITAL; HUMANS; KIDNEY; PHENOTYPE;

EID: 33745634898     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31289     Document Type: Letter

References (9)

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