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A Case of Ring Chromosome 13 Syndrome with Jejunal Atresia and Hearing Loss.
Jin Hee Lee, Jung Hyun Lee, Chung Sik Chun
Neonatal Med. 2006;13(1):149-153.   Published online May 1, 2006

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Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences
Clinical Genetics. 2002;62(5):415-417   Crossref logo

Aural atresia, microtia, complex heart defect, and hearing loss syndrome: Additional case
American Journal of Medical Genetics. 2003;117A(1):83-84   Crossref logo

Congenital jejunal atresia associated with jejunal duplication
Journal of Pediatric Surgery. 1978;13(1):103   Crossref logo
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Jejunal atresia associated with jejunal diverticulosis
Journal of Pediatric Surgery Case Reports. 2018;32:68-71   Crossref logo
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The Combination of Gastroschisis, Jejunal Atresia, and Colonic Atresia in a Newborn
Case Reports in Pediatrics. 2015;2015:1-4   Crossref logo
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Congenital duodenal and multiple jejunal atresia with malrotation in a patient with Down syndrome
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Cutis Tricolor Parvimaculata in Two Patients with Ring Chromosome 15 Syndrome
Pediatric Dermatology. 2011;28(6):670-673   Crossref logo

Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: a case report
Journal of Medical Case Reports. 2011;5(1):   Crossref logo
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Management of hearing loss and the normal ear in cases of unilateral Microtia with aural atresia
The Laryngoscope. 2015;126(6):1470-1474   Crossref logo
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Ring chromosome 13 syndrome
Clinical Genetics. 2008;7(3):203-208   Crossref logo