SCOPUS 정보 검색 플랫폼

Clinical Dysmorphology

Volumn 5, Issue 3, 1996, Pages 249-253

Setleis syndrome: Autosomal recessive or autosomal dominant inheritance?

(2) Al Gazali, L I a Al Talabani, J b

a UNITED ARAB EMIRATES UNIVERSITY (United Arab Emirates)

b Abu Dhabi Health Services Company SEHA (United Arab Emirates)

Author keywords

autosomal dominant; autosomal recessive; consanguinity; Setleis syndrome

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CONSANGUINEOUS MARRIAGE; FACE MALFORMATION; FAMILY; FEMALE; HUMAN; INFANT; MALE; OMAN; PEDIGREE; PRIORITY JOURNAL; SCAR; SKIN DISEASE;

ADULT; CONSANGUINITY; FACE; FEMALE; GENES, DOMINANT; GENES, RECESSIVE; HUMANS; INFANT, NEWBORN; MALE; PEDIGREE; SKIN DISEASES; SYNDROME;

EID: 0029793789 PISSN: 09628827 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (17)

References (8)

1
- 0026884216
- Setleis (bitemporal 'forceps marks') syndrome in a German family: Evidence for autosomal dominant inheritance
- Artlich A, Schwinger E, Meinecke P (1992): Setleis (bitemporal 'forceps marks') syndrome in a German family: Evidence for autosomal dominant inheritance. Clin Dysmorph 1: 157-160.
- (1992) Clin Dysmorph , vol.1 , pp. 157-160
- Artlich, A.¹ Schwinger, E.² Meinecke, P.³

2
- 0024844937
- Expanded phenotype and ethnicity in Setleis syndrome
- Clark RD, Golabi M, Lacassie Y, Hall B, Seto S (1989): Expanded phenotype and ethnicity in Setleis syndrome. Am J Med Genet 34: 354-357.
- (1989) Am J Med Genet , vol.34 , pp. 354-357
- Clark, R.D.¹ Golabi, M.² Lacassie, Y.³ Hall, B.⁴ Seto, S.⁵

3
- 0025860976
- Focal facial dermal dysplasia: Two familial cases
- Di Lernia V, Neri I, Patrizi A (1991): Focal facial dermal dysplasia: Two familial cases. J Am Acad Dermatol 25: 389-391.
- (1991) J Am Acad Dermatol , vol.25 , pp. 389-391
- Di Lernia, V.¹ Neri, I.² Patrizi, A.³

4
- 0023260088
- Autosomal recessive inheritance in the Setleis 'forceps marks' syndrome
- Marion RW, Chitayat D, Hutcheon G, Goldberg R, Shprintzen RH, Cohen MM (1987): Autosomal recessive inheritance in the Setleis 'forceps marks' syndrome. Am J Dis Child 141: 895-897.
- (1987) Am J Dis Child , vol.141 , pp. 895-897
- Marion, R.W.¹ Chitayat, D.² Hutcheon, G.³ Goldberg, R.⁴ Shprintzen, R.H.⁵ Cohen, M.M.⁶

5
- 0029071318
- Autosomal dominant inheritance of Setleis syndrome
- Masuno M, Imaizumi K, Makita Y, Nakamura M, Kuroki Y (1995): Autosomal dominant inheritance of Setleis syndrome. Am J Med Genet 57: 57-60.
- (1995) Am J Med Genet , vol.57 , pp. 57-60
- Masuno, M.¹ Imaizumi, K.² Makita, Y.³ Nakamura, M.⁴ Kuroki, Y.⁵

6
- 0016119598
- Bitemporal aplasia cutis congenita occurrence with other cutaneous abnormalities
- Rudolph RI, Schwartz W, Leyden JJ (1974a): Bitemporal aplasia cutis congenita occurrence with other cutaneous abnormalities. Arch Dermatol 110: 615-618.
- (1974) Arch Dermatol , vol.110 , pp. 615-618
- Rudolph, R.I.¹ Schwartz, W.² Leyden, J.J.³

7
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- Emendation to bitemporal aplasia cutis congenita
- Rudolph RI, Schwartz W, Leyden JJ (1974b): Emendation to bitemporal aplasia cutis congenita. Arch Dermatol 110: 636.
- (1974) Arch Dermatol , vol.110 , pp. 636
- Rudolph, R.I.¹ Schwartz, W.² Leyden, J.J.³

8
- 0001216317
- Congenital ectodermal dysplasia of the face
- Setleis H, Kramer B, Valcarcel M, Einhorn AH (1963): Congenital ectodermal dysplasia of the face. Pediatrics 32: 540-547.
- (1963) Pediatrics , vol.32 , pp. 540-547
- Setleis, H.¹ Kramer, B.² Valcarcel, M.³ Einhorn, A.H.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.