A patient with a de novo 11q24.2→qTER deletion

Genetic Counseling

Volumn 15, Issue 1, 2004, Pages 1-7

  Spruijt, L ^a   Fryns, J P ^a,b   Hanekom, J ^c   Engelen, J J M ^a,d   Alofs, M ^a   Albrechts, J C M ^a   Schrander Stumpel, Connie T R M ^a,d  

^a MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^c LAURENTIUS HOSPITAL   (Netherlands)

^d MAASTRICHT UNIVERSITY   (Netherlands)

Author keywords

11q monosomy; Jacobsen syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 10Q; CHROMOSOME 11; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CYTOGENETICS; FEMALE; GENE DELETION; HEART VENTRICLE SEPTUM DEFECT; HUMAN; JACOBSEN SYNDROME; KARYOTYPE; MENTAL DEFICIENCY; METAPHASE; MONOSOMY; MULTIGENE FAMILY; THROMBOCYTOPENIA;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 11; CRANIOSYNOSTOSES; CYTOGENETICS; FEMALE; GENE DELETION; HUMANS; KARYOTYPING; PHENOTYPE; TRANSLOCATION, GENETIC;

EID: 1642546284     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

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