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Ophthalmic Genetics

Volumn 27, Issue 2, 2006, Pages 63-65

Peters anomaly in association with multiple midline anomalies and a familial chromosome 4 inversion

(3) Neilan, Edward a Pikman, Yana a Kimonis, Virginia E a

a BOSTON CHILDREN S HOSPITAL (United States)

Author keywords

Meningocele; Peters anomaly

Indexed keywords

ANAMNESIS; ARTICLE; CAPILLARY HEMANGIOMA; CASE REPORT; CHILD DEVELOPMENT; CHROMOSOME 4Q; CHRONIC OTITIS MEDIA; CLEFT LIP; CLEFT PALATE; CONDUCTION DEAFNESS; DISEASE ASSOCIATION; ECHOCARDIOGRAPHY; ENCEPHALOMENINGOCELE; FAMILY HISTORY; FATHER; GENETIC ANALYSIS; GENETIC ASSOCIATION; HEART ATRIUM SEPTUM DEFECT; HEART DISEASE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; MALE; MICROPHTHALMIA; MYRINGOTOMY; NEUROIMAGING; PARACENTRIC CHROMOSOME INVERSION; PATENT DUCTUS ARTERIOSUS; PETERS ANOMALY; PIGMENTED NEVUS; PRIORITY JOURNAL; SCALP; SIBLING; SKULL DEFECT; SPEECH DISORDER; SPEECH THERAPY;

ABNORMALITIES, MULTIPLE; ANTERIOR CHAMBER; CHROMOSOMES, HUMAN, PAIR 4; CLEFT LIP; CLEFT PALATE; EAR; EYE ABNORMALITIES; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INVERSION, CHROMOSOME; MAGNETIC RESONANCE IMAGING; MALE; MENINGOCELE; OTITIS MEDIA;

EID: 33745058745 PISSN: 13816810 EISSN: 17445094 Source Type: Journal
DOI: 10.1080/13816810600678139 Document Type: Article

Times cited : (13)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.