Literature DB >> 14210861

HOLOPROSENCEPHALY: A CASE REPORT WITH NO EXTRACRANIAL ABNORMALITIES AND NORMAL CHROMOSOME COUNT AND KARYOTYPE.

K BISHOP, J M CONNOLLY, C H CARTER, D G CARPENTER.   

Abstract

Keywords:  ABNORMALITIES; AMINO ACID METABOLISM; ANOXIA; BRAIN DISEASES; CEREBROSPINAL FLUID PROTEINS; CHROMATOGRAPHY; CHROMOSOME ABNORMALITIES; CLEFT LIP; CLEFT PALATE; CONVULSIONS; DIAGNOSIS, DIFFERENTIAL; EAR, EXTERNAL, DEFORMITY; ELECTROENCEPHALOGRAPHY; GENETICS, HUMAN; HEMANGIOMA; INFANT, NEWBORN; MENTAL RETARDATION; PATHOLOGY; URINE

Mesh:

Substances:

Year:  1964        PMID: 14210861     DOI: 10.1016/s0022-3476(64)80405-4

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  2 in total

1.  What is the incidence of holoprosencephaly?

Authors:  E S Saunders; D Shortland; P M Dunn
Journal:  J Med Genet       Date:  1984-02       Impact factor: 6.318

2.  Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.

Authors:  V Váradi; L Szabó; Z Papp
Journal:  J Med Genet       Date:  1980-04       Impact factor: 6.318

  2 in total

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