A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects

Genomics

Volumn 79, Issue 4, 2002, Pages 493-498

  Spitz, François ^a   Montavon, Thomas ^a   Monso Hinard, Christine ^b   Morris, Michael ^c   Ventruto, Maria Luisa ^a   Antonarakis, Stylianos ^a   Ventruto, Valerio ^a   Duboule, Denis ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

^b GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^c INSTITUTE OF GENETICS AND BIOPHYSICS ADRIANO BUZZATI TRAVERSO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ANIMAL TISSUE; ARTICLE; BONE RADIOGRAPHY; CHROMOSOME TRANSLOCATION 2; CHROMOSOME TRANSLOCATION 8; CONTROLLED STUDY; EMBRYO; FLUORESCENCE IN SITU HYBRIDIZATION; FOREARM; GENE CLUSTER; GENE CONTROL; GENE DISRUPTION; HOMEOBOX; HUMAN; HUMAN CELL; INVERSE POLYMERASE CHAIN REACTION; ITALY; LIMB MALFORMATION; MESOMELIC DYSPLASIA; MOLECULAR CLONING; MORPHOGENESIS; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; VERTEBRA MALFORMATION;

ANIMALIA;

EID: 0036209163     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2002.6735     Document Type: Article

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