SCOPUS 정보 검색 플랫폼

Volumn 8, Issue 1, 1999, Pages 15-18

Two brothers with varying combinations of severe developmental delay, epilepsy, microcephaly, tetralogy of fallot and hydronephrosis

(6) Ryan, A a,e,f Burn, J a Court, S b Jackson, T a Clayton Smith, J c Barwick, D d

a Department of Human Genetics ^* (United Kingdom)

b QUEEN ELIZABETH HOSPITAL (United Kingdom)

c ST MARY S HOSPITAL (United Kingdom)

d ROYAL VICTORIA INFIRMARY (United Kingdom)

e Hunter Genetics (Australia)

f Hunter Health (Australia)

Author keywords

Angelman syndrome; Epilepsy; Mental retardation

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CYTOGENETICS; DEVELOPMENTAL DISORDER; EPILEPSY; FALLOT TETRALOGY; FEMALE; GENETIC DISORDER; HAPPY PUPPET SYNDROME; HUMAN; HYDRONEPHROSIS; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; MICROCEPHALY; MOLECULAR GENETICS; PRIORITY JOURNAL;

EID: 0033009870 PISSN: 09628827 EISSN: None Source Type: Journal
DOI: 10.1097/00019605-199901000-00004 Document Type: Article

Times cited : (4)

References (6)

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2
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6
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.