2.14 参考资料

1.Adalsteinnson S: Establishment of equilibrium for the dominant lethal gene for Manx taillessness in cats.Theoret Appl Genet 58:49-53,1980.

2.Baker HJ and Lindsey JR:Feline GM1 gan-gliosidosis. Am J Pathol 74:649-652,1974.

3.Barnett KC and Gurger IH:Taurine deficiency retinopathy in the cat.J Small Anim Pract 21:521-534,1980.

4.Barnett KC and Curtis R: Autosomal dominant progressive retinal atrophy in Abyssinian cats.J Hered 76:168-170,1985.

5.Bauer JE and Verlander JW:Congenital lipopro-tein lipase deficiency in hyperlipemic kitten siblings.Vet Clin Pathol 13:7-11, 1984.

6.Bellhorn RW and Fischer CA:Feline central ret-inal degeneration. JAVMA 157:842-849, 1970.

7.Benirschke K et al:Trisomy in a feline fetus.Am J Vet Res 35:27-259,1974.

8.Bergsma DR and Brown KS:White fur,blue eyes and deafness in the domestic cat.J Hered 62:171-185,1971.

9.Bistner SI et al:Hereditary corneal dystrophy in the Manx cat: a preliminary report. Invest Op-hthalmol 15:15-26,1976.

10.Bland van den Berg P et al: A suspected lyso-somal storage disease in Abyssinian cats.I. Genetic and clinical pathological aspects.J So Afr Vet Med Assn 48:195-199,1977.

11.Bosher SK and Hallpike CS: Observations of the histopathological features, development and pathogenesis of the inner ear degeneration of deaf white cats.Proc Roy Soc Lond B 162:147-170,1965.

12.Bosher SK and Hallpike CS: Obeervations of the histogenesis of the inner ear degeneration of the deaf white cat.J Laryngol 80:222-235,1966.

13.Boyce JT et al: Familial renal amyloidosis in Abyssinian cats. Vet Pathol 21:33-38, 1984.

14.Burditt LJ et al:Biochemical stdies on a case of feline mannosidosis. Biochem J 189:467-473,1980.

15.Carlisle JL:Feline retinal atrophy.Vet Record 108:311,1981.

16.Centerwall WR and Benirschke K:Male tor-toiseshell and calico cats. J Hered 64:272-278,1973.

17.Chapman VA and Zeiner FN: The anatomy of polydactylism in cats with observations on genetic control.Anat Record 141:205-217,1961.

18.Chastain CB et al: The 38,XX/39,XXY genotype in cats.Compend Cont Ed Pract Vet 10:18-22, 1988.

19.Chew DJ et al:Renal amyloidosis in related Abyssinian cats. JAVMA 181:140-142,1982.

20.Chu EHY et al:Triploid-diploid chimerism in a male tortoiseshell cat.Cytogenetics 3:1-18,1964.

21.Clifford DH et al: Congenital achalasia of the oesophagus in four cats of common ancestry.JAVMA 158:1554-1560,1971.

22.Collier LL et al: Ocular manifestations of the Chediak-Higashi syndrome in four species of animals.JAVMA 175:587-590,1979.

23.Collier LL et al: A clinical description of der-matosparaxis in a Himalayan cat. Feline Pract 10(5):25-36,1980.

24.Cooper ML and Blasdel GG:Regional variation in the representation of the visual field in the visual cortex of the Siamese cat.J Comp Neurol 193:237-253,1980.

25.Cooper ML and Pettigrew JD: The reti-nophthalamic pathways in Siamese cats.J Comp Neu-rol 187:313-348,1979.

26.Cork LC et al: GM2 ganglioside lysosomal stor-age disease in cats. Science 196:1014-1017,1977.

27.Cork LC et al: The pathology of feline GM2gangliosidosis.Am J Pathol 90:723-734,1978.

28.Cotter SM et al: Hemophilia A in three unre-lated cats. JAVMA 172:166-168,1978.

29.Counts DF et al: Dermatosparaxis in a Himala-yan cat. I. Biochemical studies of dermal collagen.J Invest Dermatol 74:96-99,1980.

30.Creel D et al:Retinal projections in tyrosinase negative albino cats. J Neurosci 2:907-911, 1982.

31.Creel D et al: Abnormal retinal projections in cats with the Chediak-Higashi syndrome.Invest Op-hthalmol Vis Sci 23:798-801,1982.

32.Crowell WA et al:Polycystic renal disease in re-lated cats.JAVMA 175:286-288, 1979.

33.Danforth CH:Heredity of polydactyly in the cat.J Hered 38:107-112,1947.

34.Danforth CH:Morphology of the feet in poly-dactyl cats.Am J Anat 80:143-171,1947.

35.Davies M and Gill I: Congenital patellar luxa-tion in the cat. Vet Record 121:474-475,1987.

36.DeForest ME and Basrur PK: Malformations and the Manx syndrome in cats. Can Vet J 20:304-314,1979.

37.Desnick RJ,in Holzworth J:Diseases of the Cat.Saunders,Philadelphia,1987. pp 808-819.

38.Desnick RJ et al, in Desnick RJ et al:Animal Models of Inherited Metabolic Diseases. Liss,New York, 1982. pp 27-65.

39.DiBartola SP et al:Pedigree analysis of Abys-sinian cats with familial amyloidosis. Am J Vet Res 47:2666-2668,1986.

40.Dodds WJ:Inherited bleeding disorders.Canine Pract 5(2):49-58,1978.

41.Dodds WJ: Second international registry of ani-mal models of thrombosis and haemorrhagic diseases.ILAR News 24:R1-R50,1981.

42.Donovan A: Postnatal development of the cat retina.Exp Eye Res 5:249-254,1966.

43.Dyte CE et al: Standardized genetic nomencla-ture for the domestic cat. J Hered 59:39-40, 1968.

44.Elverland HH and Mair IWS: Heredity deaf-ness in the cat. An electron microscopic study of the spiral ganglion. Acta Otolaryngol 90:360-369,1980.

45.Elverland HH et al:Heredity deafness in the cat.Free amino acid and sugar content in the peri-lymph.J Oto Rhino Laryngol 39:241-246, 1977.

46.Farrell DF et al: Feline GM1 gangliosidosis:biochemical and ultrastructural comparisons with the disease in man. J Neuropathol Exp Neurol 32:1-18,1973.

47.Flecknell PA and Gruffydd-Jones TJ:Congeni-tal luxation of the patellae in the cat. Feline Pract 9(3):18-19,1979.

48.Foley CW et al: Abnormalities of Companion Animals.Iowa State Univ Press, Ames, 1979.

49.Fraser AS:A note on the growth of the rex and Angora cats. J Genet 51:237-242,1953.

50.French TW et al: A bleeding disorder (von Willebrand’s disease) in a Himalayan cat. JAVMA 190:437-439,1987.

51.Gasper PW et al: Correction of feline arylsul-phatase B deficiency (mucopolysaccharidosis VI) by bone marrow transplantation. Nature 312:467-469,1984.

52.Giddens WE Jr et al: Feline congenital erythro-poietic porphyria associated with severe anemia and renal disease. Clinical, morphologic, and biochemical studies.Am J Pathol 80:367-386,1975.

53.Glenn BL: An animal model for human disease:feline porphyria. Comp Pathol Bull 2(2):2-3,1970.

54.Glenn BL et al:Congenital porphyria in the do-mestic cat (felis catus): Preliminary investigation on inheritance patterns. Am J Vet Res 29:1653-1657,1968.

55.Green RA and White F: Feline factor XII (Hageman) deficiency.Am J Vet Res 38:893-895,1977.

56.Guillary RW et al:Do blue-eyed white cats have normal or abnormal retinofugal pathways?Invest Op-hthalmol Vis Sci 21:27-33,1981.

57.Guillery RW and Kaas JH:A study of normal and congenitally abnormal retinogenicate pojections in cats. J Comp Neurol 143:73-100,1971.

58.Harpster NK: Cardiovascular diseases of the domestic cat.Adu Vet Sci Comp Med 21:39-74,1977.

59.Haskins ME et al: The pathology of feline arylsulfatase B deficient mucopolysaccharidosis.Am J Pathol 101:657-674,1980.

60.Haskins ME et al: Mucopolysaccharidosis in a domestic short haired cat. JAVMA 175:384-387,1979.

61.Haskins ME et al: Alpha-L-iduronidase defi-ciency in a cat. Pediat Res 13:1294-1297,1979.

62.Haskins ME et al,in Desnick RH:Animal Mod-els of Inherited Metabolic Diseases. Li88,New York,1982.pp 177-201.

63.Haskins ME et al: Mucopolysaccharidosis stor-age disease in three families of cats with arylsulfatase B deficiency: leukocyte studies and carrier identifica-tion.Pediat Res 13:1203-1210,1979.

64.Hayes KC et al: Retinal degeneration associ-ated with taurine deficiency in the cat. Science 188:949-952,1975.

65.Hendy-Ibbs PM:Hairless cats in Great Britain.J Herd 75:506-507,1984.

66.Hendy-Ibbs PM:Familial feline epibulbar der-moids.Vet Record 116:13-14,1985.

67.Henricson B and Bornstein S: Hereditary um-bilical hernia in cats. Svensk Vet Tid 17:95-97, 1965.

68.Hegreberg GA and Harding JW, in Andrews EJ et al: Spontaneous Animal Models of Human Disease.Academic Press, New York, 1979.pp 158-160.

69.Hirsch VM and Cunningham JA:Hereditary anomaly of neutrophil granulation in Birman cats. Am JVet Res 45:2170-2174,1984.

70.Holbrook KA et al: Dermatosparaxis in a Hima-layan cat. II. Ultrastructural studies of dermal colla-gen. J Invest Dermatol 74:100-104, 1980.

71.Howell JM and Siegel PB:Morphologic effects of the Manx factor in cats. J Hered 57:100-104,1966.

72.Hubel DH and Wiesel TN:Aberrant visual pro-jections in the Siamese cat. J Physiol 218:33-62, 1971.

73.Jackson OF: Congenital bone lesions in cats with fold-ears.Bull Feline Advis Bur 14(4):2-4,1975.

74.James CC et al: Congenital anomalies of the lower spine and spinal cord in Manx cats.J Pathol 97:269-276,1969.

75.Jezyk PF et al:Alpha-mannosidosis in a Pers-ian cat. JAVMA 189:1483-1485,1986.

76.Jezyk PF et al:Mucopolysaccharidosis in a cat with arylsulfatase B deficiency.Science 198:834-836,1977.

77.Johnson KH: Globoid leukodystrophy in the cat. JAVMA 157:2051-2064,1970.

78.Johnston SD et al: X chromosome monosomy (37,XO) in a Burmese cat with gonadal dysgenesis.JAVMA 182:986-989,1983.

79.Jones BR et al: PeripheraI neuropathy in cats with inherited primary hyperchylomicronemia.Vet Re-cord 119:268-272,1986.

80.Jones BR et al: Inherited hyperchylo-micronemia in the cat. Feline Pract 16(5):7-12,1986.

81.Jones BR et al: Occurrence of idiopathic, famil-ial hyperchylomicronemia in a cat. Vet Record 112:543-547,1983.

82.Kaas JH and Guillery RW:The transfer of ab-normal visual field representations from the dorsal lateral geniculate nucleus to the visual cortex in Sia-mese cats. Brain Res 59:61-95,1973.

83.Kalil RE et al:Anomalous retinal pathways in the Siamese cat. Science 174:302-305,1971.

84.Kier AB et al:The inheritance pattern of factor XII (Hageman) deficiency in domestic cats. Can J Comp Med 44:309-314,1980.

85.Kramer JW et al:The Chediak-Higashi syn-drome of cats. Lab Invest 36:554-562,1977.

86.Lange AL et al:A suspected lysosomal storage disease in Abyssinian cats. II. Histopathological and ultrastructural aspects.J So Afr Vet Med Assn 48:201-209,1977.

87.Latimer KS et al: Pelger-Huët anomaly in cats.Vet Pathol 22:370-374, 1985.

88.Leipold HW et al:Congenital defects of the cau-dal vertebral column and spinal cord in Manx cats.JAVMA 164:520-523,1974.

89.Letard E: La constitution d’un type ethnique disparu. Sur une famille de chats nus. Rec Med Vet 114:5-13,1938.

90.Leventhal AG and Creek DJ:Retinal projec-tions and functional architecture of cortical areas 17and 18 in the tyrosinase negative albino cat.J Neu-rosci 5:795-807, 1985.

91.Leventhal AG et al:Abnormal visual pathways in normally pigmented cats that are heterozygous for albinism.Science 229:1395-1397,1985.

92.Levick WR et al: Retinal ganglion cells and optic decussation of white cats. Vision Res 20:1001-1006,1980.

93.Little CC:Four-ears, a recessive mutation in the cat.J Hered 48:57, 1957.

94.Liu S-K:Pathology of feline heart disease.Vet Clin No Am 7:323-339,1977.

95.Livingston ML:A possible hereditary influence in feline urolithiasis. VM/SAC 60:705,1965.

96.Loevy HT:Cytogenic analysis of Siamese cats with cleft palate.J Dent Res 53:453-456,1974.

97.Loevy HT and Fenyeg VL:Spontaneous cleft palate in a family of Siamese cats. Cleft Palate J 5:57-60,1968.

98.Loughman WD et al:XY/XXY bone marrow mo-saicism in three male tricolor cats.Am J Vet Res 31:307-314,1970.

99.Mair IWS:Hereditary deafness in the white cat.Acta Otolaryngol (Suppl) 314, 1973.

100.Mair IWS and Elverland HH:Hereditary deaf-ness in the cat. An electron microscopic study of the stria vascularis and Reissner’s membrane.Arch Oto Rhino Laryngol 217:199-217,1977.

101.Martin AH:A congenital defect in the spinal cord of the Manx cat. Vet Pathol 8:232-239,1971.

102.Mason K:A hereditary disease in Burmese cats manifested as an episodic weakness with head nodding and neck ventroflexion. JAAHA 24:147-151,1988.

103.McFeely RA et al: Chromosome studies in 14cases of intersex in domestic mammals.Cytogenetics 6:242-253,1967.

104.McGovern MM et al:Animal model studies of allelism:characterization of arylsulfatase B mutations in homoallelic and heteroallelic (genetic compound)homozygotes with feline mucopolysaccharidosis VI.Genetics 110:733-749,1985.

105.McGovern MM et al:An improved method for heterozygous identification in feline and human mucopolysaccharidosis VI,arylsulfatase B deficiency.Enzyme 26:206-210,1981.

106.McGovern MM et al: Purification and proper-ties of feline and human arylsulfatase B isozymes.J Biol Chem 257:12605-12610, 1982.

107.Migaki G,in Deanick RH:Animal Models of Inherited Metabolic Diseases. Liss,New York,1982.pp 473-501.

108.Moran C et al: Fertile male tortoiseshell cats.J Hered 75:397-402,1984.

109.Moutschen J:Quelques particularities heredi-taires du chat siamois. Nat Belges 31:200-203, 1950.

110.Narfstrom K: Hereditary progressive retinal atrophy in the Abyssinian cat.J Hered 74:273-276,1983.

111.Narfstrom K and Nilsson EG:Degenerative Retinal Disorders: Clinical and Laboratory Investiga-tions.Liss, New York,1987.pp 349-368.

112.Narfstrom K:Progressive retinal atrophy in the Abyssinian cat. Invest Ophthalmol Vis Sci 26:193-200,1985.

113.Narfstrom K: Retinal degeneration in a strain of Abyssinian cats.Linkoping Univ Med Diss No 208:91,1985.

114.Narfstrom K et al:Progressive retinal atrophy in the Abyssinian cat: studies of the DC-recorded electroretinogram and the standing potential of the eye.Brit J Ophthalmol 69:618-623, 1985.

115.Noden DM and Evans HE: Inherited homeotic midfacial malformations in Burmese cats.J Craniofa-cial Devel Biol 2:249-266,1986.

116.Norby DE et al: An XO cat. Cytogenet Cell Genet 13:448-453,1974.

117.Norby DE and Thuline HC:Inherited tremor in the domestic cat. Nature 227:1262-1263,1970.

118.Paasch H and Zook BC:The pathogenesis of endocardial fibroelastosis in Burmese cats. Lab Invest 42:197-204,1980.

119.Patterson DF et al: Models of human genetic disease in domestic animals. Advance Hum Genet 12:263-339,1982.

120.Patterson DF and Minor RR:Hereditary fra-gility and hyperextensibility of the skin of cats.Lab Invest 37:170-179,1977.

121.Pearson H et al: Pyloric stenosis and oesopha-geal dysfunction in the cat. J Small Anim Pract 15:487-501,1974.

122.Prieur DJ and Collier LL:Inheritance of the Chediak-Higashi syndrome in cats. J Hered 72:175-177,1981.

123.Prieur DJ and Collier LL:Morphologic basis of inherited coat colour dilutions of cats.J Hered 72:178-182,1981.

124.Pujol R et al:Primary neural disorders in the deaf white cat’s cochlea.Acta Otolaryngol 83:59-64,1977.

125.Pyle RL et al:XXY sex chromosome constitu-tion in a Himalayan cat with tortoiseshell points.J Hered 62:220-221,1971.

126.Rebillard M et al:Variability of the hereditary deafness in the white cat. II.Histology.Hear Res 5:189-200,1981.

127.Rebillard M et al: Variability of the hereditary deafness in the white cat.I.Physiology.Hear Res 5:179-187,1981.

128.Robinson R:German rex: a rexoid coat mu-tant in the cat. Genetica 39:351-352,1968.

129.Robinson R:Devon rex: a third rexoid coat mutant in the cat. Genetica 40:597-599,1969.

130.Robinson R:Gene assortment and preferential mating in the breeding of German fancy cats.Heredity 25:207-216,1970.

131.Robinson R:The rex mutants of the domestic cat.Genetica 42:466-468,1971.

132.Robinson R:Oregon rex:a fourth rexoid coat mutant in the cat. Genetica 43:236-238,1972.

133.Robinson R: The Canadian hairless or Sphinx cat.J Hered 64:47-48,1973.

134.Robinson R:Genetic aspects of umbilical her-nia incidence in cats and dogs. Vet Record 100:9-10,1976.

135.Robinson R:Genetics for Cat Breeders.2nd ed.Pergamon Press, London, 1977.

136.Robinson R:A third hypotrichosis in thedo-mestic cat.Genetica 55:39-40,1981.

137.Robinaon R:Dutch rex:a fifth rexoid coat mu-tant in the cat. Genetica 57:217-218,1982.

138.Robinson R:Fertile male tortoiseshell cats.J Hered 76:137-138,1985.

139.Robinson R: Unpublished data,1986.

140.Rubin LF:Hereditary cataract in Himalayan cats.Feline Pract 16(4):14-15,1986.

141.Rubin LF and Lipton DE: Retinal degenera-tion in kittens.JAVMA 162:467-469,1973.

142.Sandstrom B et al:Glycogenesis of the central nervous system in the cat.Acta Neuropath 14:194-200,1969.

143.Saperstein G et al: Congenital defects in do-mestic cats.Feline Pract 6(4):18-43, 1976.

144.Searle AG:Hereditary“split-hand” in the do-mestic cat.Annal Eugen 17:279-282,1953.

145.Searle AG and Jude AC:The rex type of coat in the domestic cat.J Genet 54:506-512,1956.

146.Severin GA:Congenital and acquired heart disease.JAVMA 151:1733-1736,1967.

147.Shatz CJ and Kliot M: Prenatal misrouting of the retinogeniculate pathway in Siamese cats.Nature 300:525-529,1982.

148.Silson M and Robinson R:Hereditary hydro-cephalus in the cat. Vet Record 84:477,1969.

149.Sponenberg DP and Graf-Webster E:Heredi-tary meningoencephalocele in Burmese cats.J Hered 77:60,1986.

150.Suomalainen E: The inheritance of tailless-ness in the cat.Novant Anni Deel Leggi Mendeliane 14:220-234,1956.

151.Thibos LN et al: Ocular pigmentation in white and Siamese cats. Invest Ophthalmol Vis Sci 19:475-486,1980.

152.Thomsen PD et al:Fertility in two cats with X-chromosome mosaicism and unilateral ovarian dys-genesis.J Reprod Fert 80:43-47, 1987.

153.Tobias G: Congenital porphyria in a cat.JAVMA 145:462-463,1964.

154.Todd NB: The inheritance of taillessness in Manx cats.J Hered 52:228-232,1961.

155.Turner P and Robinaon R:Melanin inhibitor:a dominant gene in the domestic cat. J Hered 71:427-428,1980.

156.Turner P et al: Blue-eyed albino: a new albino allele in the domestic cat. Genetica 56:71-73,1981.

157.Vandevelde M et al: Hereditary neurovisceral mannosidosis associated with mannosidase deficiency in a family of Persian cats.Acta Neuropathol 58:64-68,1982.

158.Vawer GD: Corneal mummification in colour-point cats. Vet Record 109:413,1981.

159.Vine DT et al: Feline mucopolysaccharidosis IV:purification and characterizatin of the residual arylsulfatase B activity.Am J Hum Genet 33:916-927,1981.

160.Voaden MJ et al: Degenerative Retinal Disor-ders:Clinical and Laboratory Investigations.Liss,New York,1987.pp 369-380.

161.Weber SE et al: Pelger-Huët anomaly of gran-ulocytic leukocytes in two feline littermates.Feline Pract 11(1):44-47, 1981.

162.Wenger DA et al: Niemann-Pick disease: age-netic model in Siamese cats. Science 208:1471-1473,1980.

163.West CD and Harrison JM: Transneural cell atrophy in the congenitally white cat.J Comp Neurol 151:377-398,1973.

164.West-Hyde L and Buyukmihci N:Photorecep-tor degeneration in a family of cats. JAVMA 181:243-247,1982.

165.William-Jones BG:Arrested development of the long bones of the forelimbs in a female cat.Vet Re-cord 56:449,1944.

166.Woodard JC et al:Feline hereditary neuro-axonal dystrophy. Am J Pathol 74:551-566, 1974.

167.Zook BC et al:The comparative pathology of primary endocardial fibroelastosis in Burmese cats.Virchow Arch (Pathol Anat) 390:211-227,1981.

168.Zook BC et al: Encephalocele and other con-genital craniofacial anomalies in Burmese cats.VM/SAC 78:695-701,1983.

169.Giger U et al: Familial glycogen storage dis-ease Type IV in Norwegian Forest Cats.Proc 8th Ann ACVIM Forum,1990.

170.Biller DS et al:Polycystic kidney disease in a family of Persian cats. JAVMA 196:1288-1290, 1990.

171.Cohn LA and Meuten DJ:Bone fragility in a kitten: An osteogenesis imperfecta-like syndrome.JAVMA 197:98-100, 1990.