Phenotypic overlapping of autosomal trisomy syndromes and its significance.

Balakrishnan, S; Puri, R K; Bhargava, I

Balakrishnan, S; Puri, R K; Bhargava, I.

Indian Pediatr ; 1971 Jul; 8(7): 336-41

Article in English | IMSEAR | ID: sea-11654

Subject(s)

Abnormalities, Multiple/diagnosis; Child; Child, Preschool; Chromosome Aberrations/diagnosis; Chromosome Disorders; Chromosomes, Human, 13-15; Chromosomes, Human, 16-18; Consanguinity; Diagnosis, Differential; Hepatitis/congenital; Humans; Infant; Infant, Newborn; Phenotype; Skull/abnormalities; Trisomy

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Phenotype / Skull / Trisomy / Abnormalities, Multiple / Humans / Infant, Newborn / Child / Child, Preschool / Chromosome Aberrations / Chromosomes, Human, 13-15 Type of study: Diagnostic study Language: English Journal: Indian Pediatr Year: 1971 Type: Article

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