Literature DB >> 14148222

FAMILIAL CHROMOSOME-2, 3 TRANSLOCATION ASCERTAINED THROUGH AN INFANT WITH MULTIPLE MALFORMATIONS.

C S LEE, P BOWEN, H ROSENBLUM, L LINSAO.   

Abstract

Entities:  

Keywords:  ABNORMALITIES; CHIN; CHROMOSOME ABNORMALITIES; CLEFT PALATE; CRYPTORCHISM; EAR, EXTERNAL, DEFORMITY; GENETICS, HUMAN; HAND DEFORMITIES; HEART AUSCULTATION; HEART SEPTAL DEFECTS, ATRIAL; HEMANGIOMA; HYDRONEPHROSIS; INFANT, NEWBORN; INTESTINAL OBSTRUCTION; MONSTERS; THORACIC RADIOGRAPHY; URETER; UROGRAPHY

Mesh：

Year:  1964        PMID： 14148222     DOI： 10.1056/NEJM196407022710102

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


× No keyword cloud information.
  5 in total

Review 1.  Congenital chromosomal syndromes. A model for pathogenesis.

Authors:  R A Rohde
Journal:  Calif Med       Date:  1965-10

2.  [Familial 2-C translocation: 46,XYt(2p-;Cp+) and 46,XXCp+].

Authors:  K Bender; H Reinwein; L Z Gorman; U Wolf
Journal:  Humangenetik       Date:  1969-10

3.  New chromosomal dysmorphic syndromes. 3. Partial trisomy 3q.

Authors:  S Stengel-Rutkowski; J D Murken; V Pilar; B Dutrillaux; A Rodewald; R Goebel; R Bassermann
Journal:  Eur J Pediatr       Date:  1979-02-08       Impact factor: 3.183

4.  Congenital malformations of the central nervous system in spontaneous abortions.

Authors:  M R Creasy; E D Alberman
Journal:  J Med Genet       Date:  1976-02       Impact factor: 6.318

5.  Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

Authors:  P W Allderdice; N Browne; D P Murphy
Journal:  Am J Hum Genet       Date:  1975-11       Impact factor: 11.025
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.