A case of presumptive monosomy 21 re-diagnosed as unbalanced t(5p;21q) by FISH and review of literature

American Journal of Medical Genetics

Volumn 70, Issue 2, 1997, Pages 174-178

  Iqbal, M Anwar ^a,b   Ahmed, Mohammed Zein Seid ^c   Wu, David ^a   Sakati, Nadia ^b  

^a Laboratory Medicine   (Saudi Arabia)

^b KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^c SECURITY FORCES HOSPITAL   (Saudi Arabia)

Author keywords

5p 21q deletion syndrome; fluorescence in situ hybridization; monosomy 21

Indexed keywords

ARTICLE; CASE REPORT; CAT CRY SYNDROME; CHROMOSOME 21; CHROMOSOME 5; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION 5; CLINICAL FEATURE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INFANT; MALE; MONOSOMY; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 5; CRI-DU-CHAT SYNDROME; DIAGNOSIS, DIFFERENTIAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; MONOSOMY; TRANSLOCATION, GENETIC;

FELIS CATUS;

EID: 0030899594     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970516)70:2<174::AID-AJMG14>3.0.CO;2-G     Document Type: Article

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