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American Journal of Medical Genetics

Volumn 99, Issue 4, 2001, Pages 335-337

No evidence of dup(7)(p11.2p13) in Silver-Russell syndrome [2]

(4) Martinez, Maria Jose a Binkert, Franz a Schinzel, Albert a Kotzot, Dieter a

a UNIVERSITY OF ZURICH (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

EPIDERMAL GROWTH FACTOR RECEPTOR; SOMATOMEDIN BINDING PROTEIN 3;

CHROMOSOME 7P; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; FEMALE; GENE FREQUENCY; GENETIC LINKAGE; HUMAN; LETTER; MALE; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME;

ABNORMALITIES, MULTIPLE; ALLELES; CHILD; CHROMOSOMES, HUMAN, PAIR 7; CRANIOFACIAL ABNORMALITIES; FAMILY HEALTH; FEMALE; FETAL GROWTH RETARDATION; GENE DUPLICATION; GROWTH DISORDERS; HUMANS; LYMPHOCYTES; MALE; MICROSATELLITE REPEATS; POLYMERASE CHAIN REACTION; SYNDROME;

EID: 0035313905 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1177>3.0.CO;2-Q Document Type: Letter

Times cited : (10)

References (11)

1
- 0025651013
- Autosomal and X-chromosome imprinting
- (1990) Dev Suppl , pp. 63-72
- Cattanach, B.M.¹ Beechey, C.V.²

2
- 0030930299
- Molecular studies in 37 Silver-Russell syndrome patients: Frequency and etiology of uniparental disomy
- (1997) Hum Genet , vol.100 , pp. 415-419
- Eggermann, T.¹ Wollmann, H.A.² Kuner, R.³ Eggermann, K.⁴ Enders, H.⁵ Kaiser, P.⁶ Ranke, M.B.⁷

3
- 0032846736
- Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features in Silver-Russell syndrome
- (1999) Hum Genet , vol.105 , pp. 273-280
- Joyce, Ch.A.¹ Sharp, A.² Walker, J.M.³ Bullman, H.⁴ Temple, I.K.⁵

4
- 0033910406
- Isoform-specific imprinting of the human PEG1/MEST gene
- (2000) Am J Hum Genet , vol.66 , pp. 309-312
- Kosaki, K.¹ Kosaki, R.² Craigen, W.J.³ Matsuo, N.⁴

5
- 0028914364
- Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
- (1995) Hum Mol Genet , vol.4 , pp. 583-587
- Kotzot, D.¹ Schmitt, S.² Bernasconi, F.³ Robinson, W.P.⁴ Lurie, I.W.⁵ Llyina, H.⁶ Mehes, K.⁷ Hamel, B.C.J.⁸ Otten, B.J.⁹ Hergersberg, M.¹⁰ Werder, E.¹¹ Schönle, E.¹² Schinzel, A.¹³

6
- 0033940412
- Duplication of 7p11.2-p13, including GRB10, IN Silver-Russell syndrome
- (2000) Am J Hum Genet , vol.66 , pp. 36-46
- Monk, D.¹ Wakeling, E.L.² Proud, V.³ Hitchins, M.⁴ Abu-Mero, S.N.⁵ Stanier, Ph.⁶ Preece, M.A.⁷ Moore, G.E.⁸

7
- 0031036341
- Maternal uniparental disomy 7 in Silver-Russell syndrome
- (1997) J Med Genet , vol.34 , pp. 6-9
- Preece, M.A.¹ Price, S.M.² Davies, V.³ Clough, L.⁴ Stanier, P.⁵ Trembath, R.C.⁶ Moore, G.E.⁷

8
- 0028958731
- Familial inverted duplication 7p
- (1995) Am J Med Genet , vol.56 , pp. 184-187
- Schäfer, G.B.¹ Novak, K.² Steele, D.³ Smith, S.⁴ Zaleski, D.⁵ Pickering, D.⁶ Nelson, M.⁷ Sanger, W.⁸

9
- 0003995432
- Human cytogenetics database
- Oxford Medical Databases Series. Oxford: Oxford University Press, updated
- (1994)
- Schinzel, A.¹

10
- 0034011278
- Bialleleic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndrome
- (2000) J Med Genet , vol.37 , pp. 65-67
- Wakeling, E.L.¹ Hitchins, M.P.² Abu-Amero, S.N.³ Stanier, Ph.⁴ Moore, G.E.⁵ Preece, M.A.⁶

11
- 0028827636
- Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients
- (1995) Eur J Pediatr , vol.154 , pp. 958-968
- Wollmann, H.A.¹ Kirchner, T.² Enders, H.³ Preece, M.A.⁴ Ranke, M.B.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.