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International Journal of Pediatric Otorhinolaryngology

Volumn 68, Issue 3, 2004, Pages 353-357

The Carpenter syndrome phenotype

(4) Tarhan, Erkan a Oǧuz, Haldun a,b Şafak, Mustafa Asim a Samim, Erdal a

a ANKARA TRAINING AND RESEARCH HOSPITAL (Turkey)

b Elvankent Emlak Bankasi (Turkey)

Author keywords

ABR; Carpenter syndrome; Sensorineural hearing deficit

Indexed keywords

ACROCEPHALOPOLYSYNDACTYLY TYPE 2; ACROCEPHALOSYNDACTYLY; ACROMEGALY; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL HEART DISEASE; CRYPTORCHISM; EVOKED BRAIN STEM AUDITORY RESPONSE; FACE; FACE HYPOPLASIA; HEARING; HEARING LOSS; HIGH ARCHED PALATE; HUMAN; HYPOPLASIA; MALE; MENTAL DEFICIENCY; MICROSTOMIA; OBESITY; PERCEPTION DEAFNESS; POLYDACTYLY; PRESCHOOL CHILD; PRIORITY JOURNAL; SYNDACTYLY;

EID: 1042264002 PISSN: 01655876 EISSN: None Source Type: Journal
DOI: 10.1016/j.ijporl.2003.10.009 Document Type: Article

Times cited : (19)

References (9)

1
- 0035462128
- Oral findings in Carpenter syndrome
- Blankenstein R., Brook A.H., Smith R.N., Patrick D., Russel J.M. Oral findings in Carpenter syndrome. Int. J. Paediatr. Dent. 11:2001;352-360.
- (2001) Int. J. Paediatr. Dent. , vol.11 , pp. 352-360
- Blankenstein, R.¹ Brook, A.H.² Smith, R.N.³ Patrick, D.⁴ Russel, J.M.⁵

2
- 0025141380
- Carpenter syndrome: Marked variability of expression to include the Summit and Goodman syndromes
- Gershoni R.B. Carpenter syndrome: Marked variability of expression to include the Summit and Goodman syndromes. Am. J. Med. Genet. 35:1990;236-240.
- (1990) Am. J. Med. Genet. , vol.35 , pp. 236-240
- Gershoni, R.B.¹

3
- 0023472543
- Acrocephalopolysyndactyly Type II-Carpenter syndrome
- Cohen D.M., Green J.G., Miller J., Gorlin R.J., Reed J.A. Acrocephalopolysyndactyly Type II-Carpenter syndrome. Am. J. Med. Genet. 28:1987;311-324.
- (1987) Am. J. Med. Genet. , vol.28 , pp. 311-324
- Cohen, D.M.¹ Green, J.G.² Miller, J.³ Gorlin, R.J.⁴ Reed, J.A.⁵

4
- 0027261371
- Carpenter syndrome with normal intelligence
- Costa A.R., Pirolo L., Cohen M.M. Carpenter syndrome with normal intelligence. Am. J. Med. Genet. 47:1993;281-283.
- (1993) Am. J. Med. Genet. , vol.47 , pp. 281-283
- Costa, A.R.¹ Pirolo, L.² Cohen, M.M.³

5
- 0026622962
- Familial occurence of Summit syndrome or a variant example of Carpenter syndrome
- Pierquin G., Seligmann R., Regemorter N.V. Familial occurence of Summit syndrome or a variant example of Carpenter syndrome. Genet. Couns. 3:1992;101-105.
- (1992) Genet. Couns. , vol.3 , pp. 101-105
- Pierquin, G.¹ Seligmann, R.² Regemorter, N.V.³

6
- 1842289791
- A case of carpenter syndrome diagnosed in a 20 week old fetus with postmortem examination
- Balci S., Önol B., Eryilmaz M., Haytoǧlu T. A case of carpenter syndrome diagnosed in a 20 week old fetus with postmortem examination. Clin. Genet. 51:1997;412-416.
- (1997) Clin. Genet. , vol.51 , pp. 412-416
- Balci, S.¹ Önol, B.² Eryilmaz, M.³ Haytoǧlu, T.⁴

7
- 0026681095
- Apert syndrome with partial polydactyly
- Lefort G., Sarda P., Humeau C., Rieu D. Apert syndrome with partial polydactyly. Genet. Couns. 3:1992;107-109.
- (1992) Genet. Couns. , vol.3 , pp. 107-109
- Lefort, G.¹ Sarda, P.² Humeau, C.³ Rieu, D.⁴

8
- 0025643079
- Live birth prevelance and follow up of malformation syndromes in 27,472 newborns
- Higurashi M., Oda M., Iijama K., Iijama S., Takeshita T., Watanabe N., Yoneyama K. Live birth prevelance and follow up of malformation syndromes in 27,472 newborns. Brain Dev. 12:1990;770-773.
- (1990) Brain Dev. , vol.12 , pp. 770-773
- Higurashi, M.¹ Oda, M.² Iijama, K.³ Iijama, S.⁴ Takeshita, T.⁵ Watanabe, N.⁶ Yoneyama, K.⁷

9
- 0034522528
- Molecular-clinical spectrum of the ATR-X syndrome
- Gibbons R.J., Higgs D.R. Molecular-clinical spectrum of the ATR-X syndrome. Am. J. Med. Genet. (Semin. Med. Genet.). 97:2000;204-212.
- (2000) Am. J. Med. Genet. (Semin. Med. Genet.) , vol.97 , pp. 204-212
- Gibbons, R.J.¹ Higgs, D.R.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.