Partial deletion of 4p and 4q in a fetus with ring chromosome 4: phenotype and molecular mapping of the breakpoints.

Journal of medical genetics

Volumn 39, Issue 5, 2002, Pages

  Kocks, A ^a   Endele, S ^a   Heller, R ^a   Schroder B ^a   Schäfer, H J ^a   Stadtler C ^a   Makrigeorgi Butera, M ^a   Winterpacht, A ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 4; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME DISORDER; CHROMOSOME MAP; CONGENITAL MALFORMATION; FEMALE; FETUS; GENETICS; HUMAN; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PHENOTYPE; RING CHROMOSOME; SYNDROME; ULTRASTRUCTURE;

ABNORMALITIES, MULTIPLE; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; FETUS; HUMANS; PHENOTYPE; RING CHROMOSOMES; SYNDROME;

EID: 0036580748     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.39.5.e23     Document Type: Article

References (0)