Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster

Journal of Medical Genetics

Volumn 35, Issue 1, 1998, Pages 31-36

  Sabry, M A ^a,d   Zaki, M ^b   Abul Hassan, S J ^a   Ramadan, D G ^c   Abdel Rasool, M A ^a   Al Awadi, S A ^a   Al Saleh, Q ^b  

^a Kuwait Medical Genetics Centre   (Kuwait)

^b FARWANIYA HOSPITAL   (Kuwait)

^c AL SABAH HOSPITAL   (Kuwait)

^d NONE   (United Kingdom)

Author keywords

22q11.2 haploinsufficiency cluster; CATCH 22; Kenny Caffey syndrome

Indexed keywords

CANDIDA ANTIGEN; CD4 ANTIGEN; CD8 ANTIGEN;

ARAB; ARTICLE; B LYMPHOCYTE; CASE REPORT; CELL SUBPOPULATION; CELL TRANSFORMATION; CHROMOSOME 22Q; CONTROLLED STUDY; DIGEORGE SYNDROME; EYE MALFORMATION; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH RETARDATION; HAPLOTYPE; HUMAN; HUMAN CELL; HYPOCALCEMIA; INTRAUTERINE GROWTH RETARDATION; KENNY CAFFEY SYNDROME; MALE; METAPHASE; MULTIPLE MALFORMATION SYNDROME; NEUTROPHIL; NEWBORN; NEWBORN DEATH; OSTEOSCLEROSIS; PARATHYROID HORMONE BLOOD LEVEL; PHAGOCYTOSIS; PHENOTYPE; PRIORITY JOURNAL; STENOSIS;

CANDIDA; RAPHIA FRATER;

EID: 0031981389     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.35.1.31     Document Type: Article

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