Cri du chat syndrome

Journal of Postgraduate Medicine

Volumn 42, Issue 3, 1996, Pages 86-88

  Iyer, Sujata L ^a   Duraiswamy, Ashwath ^a   Kher, Archana S ^a   Joshi, Sucheta ^a   Bharucha, Burjor A ^a   Kanade, Sanjivini ^a  

^a KEM HOSPITAL   (India)

Author keywords

Chromosome 5; Cri du chat syndrome

Indexed keywords

ARTICLE; CASE REPORT; CAT CRY SYNDROME; CHROMOSOME 5; CHROMOSOME DELETION; DISEASE COURSE; GENETICS; HUMAN; INFANT; KARYOTYPING; NEWBORN; PATHOLOGY; PATHOPHYSIOLOGY; PHENOTYPE; TIME;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 5; CRI-DU-CHAT SYNDROME; DISEASE PROGRESSION; HUMANS; INFANT; INFANT, NEWBORN; KARYOTYPING; PHENOTYPE; TIME FACTORS;

EID: 0030177361     PISSN: 00223859     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Jones KL (Editor) Smith's Recognisable Patterns of Human Malformation Ivth Edition 1984; W B Saunders. 40-1.
2. Buyse ML (Editor) Brith Defects Encyclopedia, Centre for Birth Defects Information Service 1990; 338-39.
3. Kushwick T, Rao KW, Lamb AL. Familial 5p syndrome. Clinical Genetics 1984; 26: 472-76.
4. AEH Emery and DL Rimoin. Principles and Practice of Medical Genetics, Chruchill Livingstone Edinburgh 1983; Vol 1, Chapter 15, 186-87.
5. Wilkins LE, Nance WE Clinical heterogeneity in 80 homereared children with cri du chat syndrome. J Pediatr 1983; 102: 528-33.