SCOPUS 정보 검색 플랫폼

Prenatal Diagnosis

Volumn 24, Issue 1, 2004, Pages 69-70

Prospective prenatal diagnosis of Fraser syndrome variant in a family with negative history [2]

(4) Maruotti, G M a Paladini, D a Agangi, A a Martinelli, P a

a UNIVERSITY OF NAPLES FEDERICO II (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DIFFERENTIAL DIAGNOSIS; DIGESTIVE SYSTEM MALFORMATION; FACE MALFORMATION; FAMILY HISTORY; FEMALE; FETUS; FETUS ECHOGRAPHY; FRASER SYNDROME; HUMAN; HUMAN TISSUE; LETTER; MULTIPLE MALFORMATION SYNDROME; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ABORTION, INDUCED; ADULT; DIAGNOSIS, DIFFERENTIAL; ESOPHAGUS; FAMILY; FEMALE; HUMANS; MALE; PEDIGREE; PREGNANCY; PREGNANCY TRIMESTER, SECOND; SYNDROME; TRACHEA; ULTRASONOGRAPHY, PRENATAL;

EID: 1042278816 PISSN: 01973851 EISSN: None Source Type: Journal
DOI: 10.1002/pd.769 Document Type: Letter

Times cited : (9)

References (7)

1
- 0034912858
- Prenatal detection of Fraser syndrome without cryptophthalmos: Case report and review of the literature
- Berg C, Geipel A, Germer U, Petersen-Hansen A, Koch-Dorfler M, Gembruch U. 2001. Prenatal detection of Fraser syndrome without cryptophthalmos: case report and review of the literature. Ultrasound Obstet Gynecol 18: 76-80.
- (2001) Ultrasound Obstet Gynecol , vol.18 , pp. 76-80
- Berg, C.¹ Geipel, A.² Germer, U.³ Petersen-Hansen, A.⁴ Koch-Dorfler, M.⁵ Gembruch, U.⁶

2
- 0023767119
- Fraser syndrome (cryptophthalmos syndactyly syndrome): A review of eleven cases with postmortem findings
- Boyd PA, Kelling JW, Lindenbaum RH. 1988. Fraser syndrome (cryptophthalmos syndactyly syndrome): a review of eleven cases with postmortem findings. Am J Med Genet 31: 159-168.
- (1988) Am J Med Genet , vol.31 , pp. 159-168
- Boyd, P.A.¹ Kelling, J.W.² Lindenbaum, R.H.³

3
- 0025058360
- Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and new-born
- Ramsing M, Rehder H, Holzgreve W, Meinecke P, Lenz W. 1990. Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and new-born. Clin Genet 37: 84-96.
- (1990) Clin Genet , vol.37 , pp. 84-96
- Ramsing, M.¹ Rehder, H.² Holzgreve, W.³ Meinecke, P.⁴ Lenz, W.⁵

4
- 0036023283
- Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome
- Rousseau T, Laurent N, Thauvin-Robinet C, et al. 2002. Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome. Prenat Diagn 22(8): 692-696.
- (2002) Prenat Diagn , vol.22 , Issue.8 , pp. 692-696
- Rousseau, T.¹ Laurent, N.² Thauvin-Robinet, C.³

5
- 0024643926
- Fraser syndrome: Prenatal ultrasonic detection
- Serville F, Carles D, Broussin B. 1989. Fraser syndrome: prenatal ultrasonic detection. Am J Med Genet 32: 561-563.
- (1989) Am J Med Genet , vol.32 , pp. 561-563
- Serville, F.¹ Carles, D.² Broussin, B.³

6
- 0028095267
- Pulmonary hyperplasia in the Fraser cryptophthalmos syndrome
- Stevens CA, McClanahan C, Steck A, Shiel FO, Carey JC. 1994. Pulmonary hyperplasia in the Fraser cryptophthalmos syndrome. Am J Med Genet 52: 427-431.
- (1994) Am J Med Genet , vol.52 , pp. 427-431
- Stevens, C.A.¹ McClanahan, C.² Steck, A.³ Shiel, F.O.⁴ Carey, J.C.⁵

7
- 0022483449
- Isolated and syndromic cryptophthalmos
- Thomas IT, Frias JL, Felix V, Sanchez de Leon L, Hernandez RA, Jones MC. 1986. Isolated and syndromic cryptophthalmos. Am J Med Genet 25: 85-98.
- (1986) Am J Med Genet , vol.25 , pp. 85-98
- Thomas, I.T.¹ Frias, J.L.² Felix, V.³ Sanchez De Leon, L.⁴ Hernandez, R.A.⁵ Jones, M.C.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.