SCOPUS 정보 검색 플랫폼

Archives of Otolaryngology - Head and Neck Surgery

Volumn 127, Issue 8, 2001, Pages 913-917

Localization of the gene for familial laryngeal abductor paralysis to chromosome 6q16

(3) Manaligod, Jose M a,b Skaggs, Jennifer a Smith, Richard J H b

a UNIVERSITY OF KENTUCKY MEDICAL CENTER (United States)

b UNIVERSITY OF IOWA HOSPITALS AND CLINICS (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CHROMOSOME 6Q; CLINICAL ARTICLE; FAMILIAL DISEASE; FLUOROMETRY; GENE LOCATION; GENE LOCUS; GENETIC LINKAGE; GENETIC MARKER; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN CELL; POLYMERASE CHAIN REACTION; STRIDOR; VOCAL CORD PARALYSIS;

EID: 0034883912 PISSN: 08864470 EISSN: None Source Type: Journal
DOI: 10.1001/archotol.127.8.913 Document Type: Article

Times cited : (14)

References (19)

1
- 0030027045
- Vocal fold paralysis in infants twelve months of age and younger
- (1996) Otolaryngol Head Neck Surg , vol.114 , pp. 18-21
- Zbar, R.I.¹ Smith, R.J.²

2
- 0024427198
- A simple and efficient non-organic procedure for the isolation of genomic DNA from blood
- (1989) Nucleic Acids Res , vol.17 , pp. 8390
- Grimberg, J.¹ Nawoschik, S.² Belluscio, L.³ McKee, R.⁴ Turck, A.⁵ Eisenberg, A.⁶

3
- 0029015151
- Novel approaches to linkage mapping
- (1995) Curr Opin Genet Dev , vol.5 , pp. 335-341
- Sheffield, V.C.¹ Nishimura, D.Y.² Stone, E.M.³

4
- 0031022393
- Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis
- (1997) Hum Mol Genet , vol.6 , pp. 117-121
- Sheffield, V.C.¹ Pierpont, M.E.² Nishimura, D.³

5
- 0031910276
- Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping
- (1998) Arch Otolaryngol Head Neck Surg , vol.124 , pp. 20-24
- Chen, A.¹ Mueller, R.² Prasad, S.³

6
- 0342499587
- Strategies for multilocus linkage analysis in humans
- (1984) Proc Natl Acad Sci USA , vol.81 , pp. 3443-3446
- Lathrop, G.M.¹ Lalouel, J.M.² Julier, C.³ Ott, J.⁴

7
- 0032557735
- Familial laryngeal paralysis
- (1998) Am J Med Genet , vol.77 , pp. 277-280
- Manaligod, J.M.¹ Smith, R.J.²

8
- 0021668839
- Vocal cord palsy in pediatric practice: A review of 71 cases
- (1984) Int J Pediatr Otorhinolaryngol , vol.8 , pp. 147-154
- Emery, P.¹ Fearon, B.²

9
- 0033983814
- Pediatric vocal fold paralysis: A long-term retrospective study
- (2000) Arch Otolaryngol Head Neck Surg , vol.126 , pp. 21-25
- Daya, H.¹ Hosni, A.² Bejar-Solar, I.³ Evans, J.N.G.⁴ Bailey, C.M.⁵

10
- 0000954887
- Congenital laryngeal-abductor paralysis due to nucleus ambiguus dysgenesis in three brothers
- (1964) N Engl J Med , vol.271 , pp. 593-597
- Plott, D.¹

11
- 0018120104
- Diagnostic/genetic studies in severe mental retardation
- (1978) Birth Defects Orig Artic Ser , vol.14 , pp. 1-38
- Opitz, J.M.¹ Kaveggia, E.² Durkin-Stamm, M.³ Pendelton, E.⁴

12
- 0015814352
- Familial laryngeal abductor paralysis and psychomotor retardation
- (1973) Clin Genet , vol.4 , pp. 429-433
- Watters, G.¹ Fitch, N.²

13
- 0022352653
- Familial vocal cord dysfunction
- (1985) Pediatrics , vol.76 , pp. 750-753
- Cunningham, M.J.¹ Eavey, R.D.² Shannon, D.C.³

14
- 0017261604
- Hereditary abductor vocal cord paralysis
- (1976) Ann Otol Rhinol Laryngol , vol.85 , pp. 90-93
- Gacek, R.R.¹

15
- 0020401279
- Congenital hereditary bilateral abductor vocal cord paralysis
- (1982) Ann Otol Rhinol Laryngol , vol.91 , Issue.6 PART 1 , pp. 564-566
- Grundfast, K.M.¹ Milmoe, G.²

16
- 0019969523
- Familial laryngeal abductor paralysis with presumed autosomal dominant inheritance
- (1982) Ann Otol Rhinol Laryngol , vol.91 , Issue.3 PART 1 , pp. 323-324
- Morelli, G.¹ Mesolella, C.² Costa, F.³ Testa, B.⁴ Ventruto, V.⁵ Santulli, S.⁶

17
- 0026587045
- Distal spinal muscular atrophy with vocal cord paralysis
- (1992) J Med Genet , vol.29 , pp. 197-199
- Pridmore, C.¹ Baraitser, M.² Brett, E.M.³ Harding, A.E.⁴

18
- 0024509068
- Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: A dominant form of spinal muscular atrophy
- (1989) J Med Genet , vol.26 , pp. 105-108
- Boltshauser, E.¹ Lang, W.² Spillmann, T.³ Hof, E.⁴

19
- 0023153525
- Variants of Möbius' syndrome and central neurologic impairment: Lindeman procedure in children
- (1987) Ann Otol Rhinol Laryngol , vol.96 , pp. 93-100
- Cohen, S.R.¹ Thompson, J.W.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.