A case of ring chromosome 22 with deletion of the 22q13.3 region associated with agenesis of the corpus callosum, fornix and septum pellucidum

Prenatal Diagnosis

Volumn 24, Issue 8, 2004, Pages 635-637

  Delcán, José ^a   Orera, María ^b   Linares, Rafael ^a,c   Saavedra, Dolores ^b   Palomar, Angustias ^a  

^a UNIVERSIDAD REY JUAN CARLOS   (Spain)

^b HOSPITAL GENERAL UNIVERSITARIO GREGORIO MARAÑÓN   (Spain)

^c Anatomia y Embriologia Humana   (Spain)

Author keywords

Agenesia telencephalic commissures; Chromosomal deletion; Ring chromosome

Indexed keywords

ABORTION; ADULT; AGENESIS; AMNION FLUID ANALYSIS; ARTICLE; BRAIN FORNIX; BRAIN FORNIX AGENESIS; CASE REPORT; CENTRAL NERVOUS SYSTEM; CHROMOSOME 22; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME G BAND; CORPUS CALLOSUM AGENESIS; CYTOGENETICS; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MORPHOLOGY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RING CHROMOSOME; SEPTUM PELLUCIDUM AGENESIS;

ADULT; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 22; CORPUS CALLOSUM; FEMALE; FORNIX (BRAIN); GENE DELETION; GESTATIONAL AGE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PREGNANCY; PRENATAL DIAGNOSIS; RING CHROMOSOMES; SEPTUM PELLUCIDUM;

EID: 4243059535     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.955     Document Type: Article

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