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Clinical Genetics

Volumn 50, Issue 4, 1996, Pages 248-250

A case report of 46,XX,del (21)(q22) de novo deletion associated with Imerslund-Grasbeck syndrome

(4) Celep, Figen a,b Karagüzel, Ahmet a Aynaci, F Müjgan a Erduran, Erol a

a KARADENIZ TECHNICAL UNIVERSITY (Turkey)

b Department of Pediatrics ^* (Turkey)

Author keywords

del(21)(q22); Grasbeck syndrome; Grasbeck syndrome Imerslund; Imerslund

Indexed keywords

CYANOCOBALAMIN;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 21; CHROMOSOME 22Q; CHROMOSOME DELETION; CYANOCOBALAMIN DEFICIENCY; FEMALE; HUMAN; KARYOTYPE 46,XX; MALABSORPTION; MEGALOBLASTIC ANEMIA; PERNICIOUS ANEMIA; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 0030471488 PISSN: 00099163 EISSN: None Source Type: Journal
DOI: 10.1111/j.1399-0004.1996.tb02637.x Document Type: Article

Times cited : (9)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.