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American Journal of Medical Genetics

Volumn 100, Issue 4, 2001, Pages 331-332

Burning down DEFECT11 [1]

(5) Wuyts, Wim a Van Hul, Wim a Bartsch, Oliver b Wilkie, Andrew O M c Meinecke, Peter d

a UNIVERSITY OF ANTWERP (Belgium)

b DRESDEN UNIVERSITY OF TECHNOLOGY (Germany)

c UNIVERSITY OF OXFORD (United Kingdom)

d Altonaer Kinderkrankenhaus (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 11P; CHROMOSOME DISORDER; CROUZON SYNDROME; EXOSTOSIS; GENE DELETION; GENETIC ANALYSIS; LETTER; MENTAL DEFICIENCY; PHENOTYPE; PRIORITY JOURNAL;

CENTRAL NERVOUS SYSTEM; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 11; CRANIOFACIAL DYSOSTOSIS; EXOSTOSES, MULTIPLE HEREDITARY; HUMANS; MENTAL RETARDATION; PARIETAL BONE; SYNDROME; TERMINOLOGY;

EID: 0035873862 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.1267 Document Type: Letter

Times cited : (7)

References (10)

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2
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3
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4
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5
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7
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9
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10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.