Cri du chat syndrome determined by the 5p15.3→pter deletion - Diagnostic problems

European Journal of Medical Genetics

Volumn 49, Issue 1, 2006, Pages 87-92

  Laczmanska, Izabela ^a   Stembalska, Agnieszka ^a   Gil, Justyna ^a   Czemarmazowicz, Halina ^a   Sasiadek, Maria ^a  

^a WROCLAW MEDICAL UNIVERSITY   (Poland)

Author keywords

5p Microdeletion; 5p ; Cri du chat syndrome; FISH

Indexed keywords

ARTICLE; CASE REPORT; CAT CRY SYNDROME; CHROMOSOME ARM; CHROMOSOME DELETION 5; CORRELATION ANALYSIS; CRANIOFACIAL MALFORMATION; CYTOGENETICS; CYTOLOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HUMAN; MOLECULAR PROBE; NEWBORN; PHENOTYPE; TELOMERE;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 5; CRI-DU-CHAT SYNDROME; DEVELOPMENTAL DISABILITIES; FEMALE; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION; INFANT, NEWBORN; INVERSION, CHROMOSOME; PHENOTYPE;

EID: 32244437667     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2005.04.023     Document Type: Article

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