SCOPUS 정보 검색 플랫폼

Genetic Counseling

Volumn 10, Issue 2, 1999, Pages 151-156

Early development (5 to 48 months) in Williams syndrome, a study of 14 children

(2) Plissart, L a Fryns, J P a,b

a UNIVERSITY HOSPITALS LEUVEN (Belgium)

b CENTER FOR HUMAN GENETICS (Belgium)

Author keywords

Behavioural phenotype; Child development; Language; Williams syndrome

Indexed keywords

ARTICLE; CHILD DEVELOPMENT; CLINICAL ARTICLE; COMPREHENSION; FEMALE; HUMAN; INFANT; LANGUAGE DEVELOPMENT; MALE; MOTOR DEVELOPMENT; PRESCHOOL CHILD; WILLIAMS BEUREN SYNDROME;

AGE FACTORS; CHILD, PRESCHOOL; DEVELOPMENTAL DISABILITIES; FEMALE; FOLLOW-UP STUDIES; HUMANS; INFANT; LANGUAGE DEVELOPMENT DISORDERS; LANGUAGE TESTS; MALE; MOTOR SKILLS DISORDERS; WILLIAMS SYNDROME;

EID: 0032812163 PISSN: 10158146 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (8)

References (8)

1
- 0345657600
- Ein neues Syndrom: Supravalvulare Aortastenose, multiple periphere Pulmonalstenosen, geistige Retardierung, ahnliche Gesichtszüge und identische Zahnmissbildungen
- BEUREN A. J.: Ein neues Syndrom: supravalvulare Aortastenose, multiple periphere Pulmonalstenosen, geistige Retardierung, ahnliche Gesichtszüge und identische Zahnmissbildungen. Monatsschr. Kinderheilk., 1964, 112, 218-221.
- (1964) Monatsschr. Kinderheilk. , vol.112 , pp. 218-221
- Beuren, A.J.¹

2
- 0027185655
- Hemozygosity at the elastin locus in a developmental disorder, Williams syndrome
- EWART A.K., MORRIS C.A., ATKINSON D., JIN W., STERNES K., SPALLONE P., STOCK AD, LEPPERT M., KEATING M.,: Hemozygosity at the elastin locus in a developmental disorder, Williams syndrome. Nature Genet., 1993, 5, 11-16.
- (1993) Nature Genet. , vol.5 , pp. 11-16
- Ewart, A.K.¹ Morris, C.A.² Atkinson, D.³ Jin, W.⁴ Sternes, K.⁵ Spallone, P.⁶ Stock, A.D.⁷ Leppert, M.⁸ Keating, M.⁹

3
- 0016689490
- The Williams elfin facies syndrome: A new perspective
- JONES K.L., SMITH D. W.: The Williams elfin facies syndrome: a new perspective. J. Pediatr., 1975, 86, 718-723.
- (1975) J. Pediatr. , vol.86 , pp. 718-723
- Jones, K.L.¹ Smith, D.W.²

4
- 0021260566
- Idiopathic infantile hypercalcaemia a continuing enigma
- MARTIN N.D.T., SNODGRASS G.J.A.I., COHEN R.D.: Idiopathic infantile hypercalcaemia a continuing enigma. Arch. Dis. Childh., 1984, 59, 603-613.
- (1984) Arch. Dis. Childh. , vol.59 , pp. 603-613
- Martin, N.D.T.¹ Snodgrass, G.J.A.I.² Cohen, R.D.³

5
- 0023688145
- Natural history of Williams syndromes: Physical characteristics
- MORRIS C.A., DEMSEY S.A., LEONARD C.O., DILTS C., BLACKBURN B.L.: Natural history of Williams syndromes: physical characteristics. Pediatr., 1988, 166-168.
- (1988) Pediatr. , pp. 166-168
- Morris, C.A.¹ Demsey, S.A.² Leonard, C.O.³ Dilts, C.⁴ Blackburn, B.L.⁵

6
- 0344794785
- Das Williams-Beuren-Syndrom
- PANKAU R.: Das Williams-Beuren-Syndrom. Forum Kinderarzt., 1996, 9, 2-4.
- (1996) Forum Kinderarzt. , vol.9 , pp. 2-4
- Pankau, R.¹

7
- 0024348718
- Neurologic features of Williams and Down syndromes
- TRAUNER D.A., BELLUGI U., CHASE C.: Neurologic features of Williams and Down syndromes. Pediatr. 1989, 5, 166-168.
- (1989) Pediatr. , vol.5 , pp. 166-168
- Trauner, D.A.¹ Bellugi, U.² Chase, C.³

8
- 0001312219
- Supravalvular aortic stenosis
- WILLIAMS J.C.P., BARRAT-BOYES B.G., LOWE J.B.: Supravalvular aortic stenosis. Circulation, 1961, 24, 1311-1318.
- (1961) Circulation , vol.24 , pp. 1311-1318
- Williams, J.C.P.¹ Barrat-Boyes, B.G.² Lowe, J.B.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.