메뉴 건너뛰기




Volumn 90, Issue 4, 1999, Pages 494-498

Comparative mapping of the DiGeorge region in the dog and exclusion of linkage to inherited canine conotruncal heart defects

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; DIGEORGE SYNDROME; DOG; GENE LOCUS; GENE MAPPING; GENETIC CONSERVATION; GENETIC LINKAGE; HUMAN; INHERITANCE; NONHUMAN; PRIORITY JOURNAL; SYNTENY;

EID: 0032849944     PISSN: 00221503     EISSN: None     Source Type: Journal    
DOI: 10.1093/jhered/90.4.494     Document Type: Article
Times cited : (11)

References (44)
  • 1
    • 0031542284 scopus 로고    scopus 로고
    • Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation
    • Botta A, Lindsay EA, Jurecic V, and Baldini A, 1997. Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation. Mamm Genome 8:890-895.
    • (1997) Mamm Genome , vol.8 , pp. 890-895
    • Botta, A.1    Lindsay, E.A.2    Jurecic, V.3    Baldini, A.4
  • 2
    • 0011976169 scopus 로고
    • Isolation and characterization of a cDNA from 22q11.2 that maps to the DiGeorge syndrome critical region (DGCR)
    • Budarf ML, Baldwin S, Biegel J, McDermid H, Emanuel BS, and Driscoll D, 1992. Isolation and characterization of a cDNA from 22q11.2 that maps to the DiGeorge syndrome critical region (DGCR). Am J Hum Genet 51: A119.
    • (1992) Am J Hum Genet , vol.51
    • Budarf, M.L.1    Baldwin, S.2    Biegel, J.3    McDermid, H.4    Emanuel, B.S.5    Driscoll, D.6
  • 4
    • 0000690417 scopus 로고    scopus 로고
    • Congenital heart disease
    • Rimoin DL, Connor JM, and Pyeritz RE, eds. New York: Churchill Livingstone
    • Burn J and Goodship J, 1997. Congenital heart disease. In: Principles and practice of medical genetics (Rimoin DL, Connor JM, and Pyeritz RE, eds). New York: Churchill Livingstone; 767-801.
    • (1997) Principles and Practice of Medical Genetics , pp. 767-801
    • Burn, J.1    Goodship, J.2
  • 7
    • 0031037933 scopus 로고    scopus 로고
    • Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion
    • Digilio MC, Marino B, Giannotti A, Toscano A, and Dallapiccola B, 1997. Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion. J Med Genet 34:188-190.
    • (1997) J Med Genet , vol.34 , pp. 188-190
    • Digilio, M.C.1    Marino, B.2    Giannotti, A.3    Toscano, A.4    Dallapiccola, B.5
  • 8
    • 0029835132 scopus 로고    scopus 로고
    • Gene localization and syntenic mapping by FISH in the dog
    • Dutra AS, Mignot E, and Puck JM, 1996. Gene localization and syntenic mapping by FISH in the dog. Cytogenet Cell Genet 74:113-117.
    • (1996) Cytogenet Cell Genet , vol.74 , pp. 113-117
    • Dutra, A.S.1    Mignot, E.2    Puck, J.M.3
  • 9
    • 0000169321 scopus 로고    scopus 로고
    • The chromosome 22q11.2 deletion
    • Harvey R and Rosenthal N, eds. New York: Academic Press
    • Emanuel BD, Budarf ML, and Scambler PJ, 1998. The chromosome 22q11.2 deletion. In: Heart development (Harvey R and Rosenthal N, eds). New York: Academic Press.
    • (1998) Heart Development
    • Emanuel, B.D.1    Budarf, M.L.2    Scambler, P.J.3
  • 10
    • 0024450369 scopus 로고
    • Congenital cardiovascular malformations: Questions on inheritance
    • Baltimore-Washington Infant Study Group
    • Ferencz C, Boughman JA, Neill CA, Brenner JI, and Perry LW, 1989. Congenital cardiovascular malformations: questions on inheritance. Baltimore-Washington Infant Study Group. J Am Coll Cardiol 14:756-763.
    • (1989) J Am Coll Cardiol , vol.14 , pp. 756-763
    • Ferencz, C.1    Boughman, J.A.2    Neill, C.A.3    Brenner, J.I.4    Perry, L.W.5
  • 12
    • 0016700935 scopus 로고
    • Etiologic relations among categories of congenital heart malformations
    • Fraser FC and Hunter ADW, 1975. Etiologic relations among categories of congenital heart malformations. Am J Cardiol 36:793-796.
    • (1975) Am J Cardiol , vol.36 , pp. 793-796
    • Fraser, F.C.1    Hunter, A.D.W.2
  • 14
    • 0025826771 scopus 로고
    • San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: A review of chromosome 8 anomalies and congenital heart disease
    • Gelb BD, Towbin JA, McCabe ER, and Sujansky E, 1991. San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease. Am J Med Genet 40:471-476.
    • (1991) Am J Med Genet , vol.40 , pp. 471-476
    • Gelb, B.D.1    Towbin, J.A.2    McCabe, E.R.3    Sujansky, E.4
  • 16
    • 0029985819 scopus 로고    scopus 로고
    • Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region
    • Goldmuntz E, Wang Z, Roe BA, and Budarf ML, 1996. Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region. Genomics 33:271-276.
    • (1996) Genomics , vol.33 , pp. 271-276
    • Goldmuntz, E.1    Wang, Z.2    Roe, B.A.3    Budarf, M.L.4
  • 18
    • 0031040139 scopus 로고    scopus 로고
    • Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region
    • Gong W, Emanuel BS, Galili N, Kim DH, Roe B, Driscoll DA, and Budarf ML, 1997. Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region. Hum Mol Genet 6: 267-276.
    • (1997) Hum Mol Genet , vol.6 , pp. 267-276
    • Gong, W.1    Emanuel, B.S.2    Galili, N.3    Kim, D.H.4    Roe, B.5    Driscoll, D.A.6    Budarf, M.L.7
  • 20
    • 0030124520 scopus 로고    scopus 로고
    • Chromosomal assignment of seven genes on canine chromosomes by fluorescence in situ hybridization
    • Guevara-Fujita ML, Loechel R, Venta PJ, Yuzbasiyan-Gurkan V, and Brewer GJ, 1996. Chromosomal assignment of seven genes on canine chromosomes by fluorescence in situ hybridization. Mamm Genome 7:268-270.
    • (1996) Mamm Genome , vol.7 , pp. 268-270
    • Guevara-Fujita, M.L.1    Loechel, R.2    Venta, P.J.3    Yuzbasiyan-Gurkan, V.4    Brewer, G.J.5
  • 25
    • 0027355585 scopus 로고
    • A Macintosh program for storage and analysis of experimental genetic mapping data form recombinant inbred strains
    • Manly KF, 1993. A Macintosh program for storage and analysis of experimental genetic mapping data form recombinant inbred strains. Mamm Genome 4:303-313.
    • (1993) Mamm Genome , vol.4 , pp. 303-313
    • Manly, K.F.1
  • 27
    • 0018358812 scopus 로고
    • Conotruncal malformation complex:examples of possible monogenic inheritance
    • Miller ME and Smith DW, 1979. Conotruncal malformation complex:examples of possible monogenic inheritance. Pediatrics 63:890-893.
    • (1979) Pediatrics , vol.63 , pp. 890-893
    • Miller, M.E.1    Smith, D.W.2
  • 28
    • 0040920369 scopus 로고    scopus 로고
    • Johns Hopkins University, Baltimore, MD. MIM Number: 217095: 8.24.1998
    • Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD. MIM Number: 217095: 8.24.1998. World Wide Web URL: http:// www.ncbi.nlm.nih.gov/omim.
    • Online Mendelian Inheritance in Man, OMIM (TM)
  • 29
    • 0029257235 scopus 로고
    • One hundred and one new simple sequence repeat-based markers for the canine genome
    • Ostrander EA, Mapa FA, Yee M, and Rine J, 1995. One hundred and one new simple sequence repeat-based markers for the canine genome. Mamm. Genome 6:192-195.
    • (1995) Mamm. Genome , vol.6 , pp. 192-195
    • Ostrander, E.A.1    Mapa, F.A.2    Yee, M.3    Rine, J.4
  • 30
    • 0027243206 scopus 로고
    • Identification and characterization of dinucleotide repeat (CA)n markers for genetic mapping in dog
    • Ostrander EA, Sprague GF, and Rine J, 1993. Identification and characterization of dinucleotide repeat (CA)n markers for genetic mapping in dog. Genomics 16:207-213.
    • (1993) Genomics , vol.16 , pp. 207-213
    • Ostrander, E.A.1    Sprague, G.F.2    Rine, J.3
  • 31
    • 0014323118 scopus 로고
    • Epidemiologic and genetic studies of congenital heart disease in the dog
    • Patterson DF, 1968. Epidemiologic and genetic studies of congenital heart disease in the dog. Circ Res 23:171-202.
    • (1968) Circ Res , vol.23 , pp. 171-202
    • Patterson, D.F.1
  • 32
    • 0027537770 scopus 로고
    • A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic development: Studies in the CTD line of keeshond dogs
    • Patterson DF, Pexieder T, Schnarr WR, Navratil T, and Alaili R, 1993. A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic development: studies in the CTD line of keeshond dogs. Am J Hum Genet 52:388-397.
    • (1993) Am J Hum Genet , vol.52 , pp. 388-397
    • Patterson, D.F.1    Pexieder, T.2    Schnarr, W.R.3    Navratil, T.4    Alaili, R.5
  • 33
    • 0016168167 scopus 로고
    • Hereditary defects of the conotruncal septum in keeshond dogs: Pathologic and genetic studies
    • Patterson DF, Pyle RL, Van Mierop L, Melbin J, and Olson M, 1974. Hereditary defects of the conotruncal septum in keeshond dogs: pathologic and genetic studies. Am J Cardiol 34:187-205.
    • (1974) Am J Cardiol , vol.34 , pp. 187-205
    • Patterson, D.F.1    Pyle, R.L.2    Van Mierop, L.3    Melbin, J.4    Olson, M.5
  • 34
    • 0024156563 scopus 로고
    • Cardiac malformations in relatives of children with truncus arteriosus or interruption of the aortic arch
    • Pierpont ME, Gobel JW, Moller JH, and Edwards JE, 1988. Cardiac malformations in relatives of children with truncus arteriosus or interruption of the aortic arch. Am J Cardiol 61:423-427.
    • (1988) Am J Cardiol , vol.61 , pp. 423-427
    • Pierpont, M.E.1    Gobel, J.W.2    Moller, J.H.3    Edwards, J.E.4
  • 36
    • 0025367690 scopus 로고
    • Genetics of conotruncal malformations: Review of the literature and report of a consanguineous kindred with various conotruncal malformations
    • Rein AJ, Dollberg S, and Gale R, 1990. Genetics of conotruncal malformations: review of the literature and report of a consanguineous kindred with various conotruncal malformations. Am J Med Genet 36:353-355.
    • (1990) Am J Med Genet , vol.36 , pp. 353-355
    • Rein, A.J.1    Dollberg, S.2    Gale, R.3
  • 37
    • 0028224435 scopus 로고
    • Genetics of conotruncal malformations: Further evidence of autosomal recessive inheritance
    • Rein AJ and Sheffer R, 1994. Genetics of conotruncal malformations: further evidence of autosomal recessive inheritance. Am J Med Genet 50:302-303.
    • (1994) Am J Med Genet , vol.50 , pp. 302-303
    • Rein, A.J.1    Sheffer, R.2
  • 39
    • 0018247879 scopus 로고
    • The pathogenesis of spontaneously occurring anomalies of the ventricular outflow tract in keeshond dogs: Embryologic studies
    • Van Mierop LHS and Patterson DF, 1978. The pathogenesis of spontaneously occurring anomalies of the ventricular outflow tract in keeshond dogs: embryologic studies. Birth Defects 14:361-375.
    • (1978) Birth Defects , vol.14 , pp. 361-375
    • Van Mierop, L.H.S.1    Patterson, D.F.2
  • 40
    • 0017708248 scopus 로고
    • Hereditary conotruncal septal defects in keeshond dogs: Embryologic studies
    • Van Mierop LHS, Patterson DF, and Schnarr WR, 1977. Hereditary conotruncal septal defects in keeshond dogs: embryologic studies. Am J Cardiol 40:936-950.
    • (1977) Am J Cardiol , vol.40 , pp. 936-950
    • Van Mierop, L.H.S.1    Patterson, D.F.2    Schnarr, W.R.3
  • 41
    • 0031570343 scopus 로고    scopus 로고
    • Physical and linkage mapping of human chromosome 17 loci to dog chromosome 9 and 5
    • Werner P, Raducha MG, Prociuk U, Henthorn PS, and Patterson DF, 1997. Physical and linkage mapping of human chromosome 17 loci to dog chromosome 9 and 5. Genomics 42:74-82.
    • (1997) Genomics , vol.42 , pp. 74-82
    • Werner, P.1    Raducha, M.G.2    Prociuk, U.3    Henthorn, P.S.4    Patterson, D.F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.