-
1
-
-
0023235059
-
Incidence of cleft lip, cleft palate, and cleft lip and palate among races: A review
-
Vanderas, A.P. (1987) Incidence of cleft lip, cleft palate, and cleft lip and palate among races: a review. Cleft Palate J., 24, 216-225.
-
(1987)
Cleft Palate J.
, vol.24
, pp. 216-225
-
-
Vanderas, A.P.1
-
2
-
-
0031667418
-
Racial and ethnic variations in the prevalence of orofacial clefts in California, 1983-1992
-
Croen, L.A., Shaw, G.M., Wasserman, C.R. and Tolarova, M.M. (1998) Racial and ethnic variations in the prevalence of orofacial clefts in California, 1983-1992. Am. J. Med. Genet., 79, 42-47.
-
(1998)
Am. J. Med. Genet.
, vol.79
, pp. 42-47
-
-
Croen, L.A.1
Shaw, G.M.2
Wasserman, C.R.3
Tolarova, M.M.4
-
3
-
-
0031973930
-
Classification and birth prevalence of orofacial clefts
-
Tolarova, M.M. and Cervenka, J. ( 1998) Classification and birth prevalence of orofacial clefts. Am. J. Med. Genet., 75, 126-137.
-
(1998)
Am. J. Med. Genet.
, vol.75
, pp. 126-137
-
-
Tolarova, M.M.1
Cervenka, J.2
-
4
-
-
8044220924
-
Clinical and epidemiologic studies of cleft lip and palate in the Philippines
-
Murray, J.C., Daack-Hirsch, S., Buetow, K.H., Munger, R., Espina, L., Paglinawan, N., Villanueva, E., Rary, J., Magee, K. and Magee, W. (1997) Clinical and epidemiologic studies of cleft lip and palate in the Philippines. Cleft Palate Craniofac. J., 34, 7-10.
-
(1997)
Cleft Palate Craniofac. J.
, vol.34
, pp. 7-10
-
-
Murray, J.C.1
Daack-Hirsch, S.2
Buetow, K.H.3
Munger, R.4
Espina, L.5
Paglinawan, N.6
Villanueva, E.7
Rary, J.8
Magee, K.9
Magee, W.10
-
5
-
-
0032124365
-
Signalling interactions during facial development
-
Francis-West, P., Ladher, R., Barlow, A. and Graveson, A. (1998) Signalling interactions during facial development. Mech. Dev., 75, 3-28.
-
(1998)
Mech. Dev.
, vol.75
, pp. 3-28
-
-
Francis-West, P.1
Ladher, R.2
Barlow, A.3
Graveson, A.4
-
6
-
-
0029050592
-
Face facts: Genes, environment, and clefts
-
Murray, J.C. (1995) Face facts: genes, environment, and clefts. Am. J. Hum. Genet., 57, 227-232.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 227-232
-
-
Murray, J.C.1
-
7
-
-
84932732093
-
Thoughts on the etiology of clefts of the palate and lip
-
Fraser, F.C. (1955) Thoughts on the etiology of clefts of the palate and lip. Acta Genet., 5, 358-369.
-
(1955)
Acta Genet.
, vol.5
, pp. 358-369
-
-
Fraser, F.C.1
-
8
-
-
0024267719
-
Etiology of facial clefts: Prospective evaluation of 428 patients
-
Jones, M.C. (1988) Etiology of facial clefts: prospective evaluation of 428 patients. Cleft Palate J., 25, 16-20.
-
(1988)
Cleft Palate J.
, vol.25
, pp. 16-20
-
-
Jones, M.C.1
-
9
-
-
0032231333
-
A chromosomal deletion map of human malformations
-
Brewer, C., Holloway, S., Zawalnyski, P., Schinzel, A. and FitzPatrick, D. (1998) A chromosomal deletion map of human malformations. Am. J. Hum. Genet., 63, 1153-1159.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1153-1159
-
-
Brewer, C.1
Holloway, S.2
Zawalnyski, P.3
Schinzel, A.4
Fitzpatrick, D.5
-
10
-
-
0033361899
-
A chromosomal duplication map of malformations: Regions of suspected haplo- And triplolethality - and tolerance of segmental aneuploidy - in humans
-
Brewer, C., Holloway, S., Zawalnyski, P., Schinzel, A. and FitzPatrick, D. (1999) A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality - and tolerance of segmental aneuploidy - in humans. Am. J. Hum. Genet., 64, 1702-1708.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1702-1708
-
-
Brewer, C.1
Holloway, S.2
Zawalnyski, P.3
Schinzel, A.4
Fitzpatrick, D.5
-
11
-
-
0030880664
-
Association between non-right-handedness and cleft lip with or without cleft palate in a Chinese population
-
Wentzlaff, K.A., Cooper, M.E., Yang, P., Aston, C.P., Liu, Y.E., Melnick, M. and Marazita, M.L. (1997) Association between non-right-handedness and cleft lip with or without cleft palate in a Chinese population. J. Craniofac. Genet. Dev. Biol., 17, 141-147.
-
(1997)
J. Craniofac. Genet. Dev. Biol.
, vol.17
, pp. 141-147
-
-
Wentzlaff, K.A.1
Cooper, M.E.2
Yang, P.3
Aston, C.P.4
Liu, Y.E.5
Melnick, M.6
Marazita, M.L.7
-
13
-
-
0023013493
-
Cleft lip with or without cleft palate: Reanalysis of a three-generation family study from England
-
Marazita, M.L., Goldstein, A.M., Smalley, S.L. and Spence, M.A. (1986) Cleft lip with or without cleft palate: reanalysis of a three-generation family study from England. Genet. Epidemiol., 3, 335-342.
-
(1986)
Genet. Epidemiol.
, vol.3
, pp. 335-342
-
-
Marazita, M.L.1
Goldstein, A.M.2
Smalley, S.L.3
Spence, M.A.4
-
14
-
-
0030696739
-
Genetic epidemiology of birth defects: Nonsyndromic cleft lip and neural tube defects
-
Mitchell, L.E. (1997) Genetic epidemiology of birth defects: nonsyndromic cleft lip and neural tube defects. Epidemiol. Rev., 19, 61-68.
-
(1997)
Epidemiol. Rev.
, vol.19
, pp. 61-68
-
-
Mitchell, L.E.1
-
15
-
-
0026668465
-
Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: A reanalysis
-
Mitchell, L.E. and Risch, N. (1992) Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: a reanalysis. Am. J. Hum. Genet, 51, 323-332.
-
(1992)
Am. J. Hum. Genet
, vol.51
, pp. 323-332
-
-
Mitchell, L.E.1
Risch, N.2
-
16
-
-
0029820276
-
Genetics of nonsyndromic oral clefts revisited
-
Wyszynski, D.F., Beaty, T.H. and Maestri, N.E. (1996) Genetics of nonsyndromic oral clefts revisited. Cleft Palate Craniofac. J., 33, 406-417.
-
(1996)
Cleft Palate Craniofac. J.
, vol.33
, pp. 406-417
-
-
Wyszynski, D.F.1
Beaty, T.H.2
Maestri, N.E.3
-
17
-
-
0023176710
-
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13a and tentative assignment to chromosome 6
-
Eiberg, H., Bixler, D., Nielsen, L.S., Conneally, P.M. and Mohr, J. (1987) Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6. Clin. Genet., 32, 129-132.
-
(1987)
Clin. Genet.
, vol.32
, pp. 129-132
-
-
Eiberg, H.1
Bixler, D.2
Nielsen, L.S.3
Conneally, P.M.4
Mohr, J.5
-
18
-
-
0028797751
-
Nonsyndromic cleft lip and palate: Evidence of linkage to a microsatellite marker on 6p23
-
Carinci, F., Pezzetti, F., Scapoli. L., Padula, E., Baciliero, U., Curioni, C. and Tognon, M. (1995) Nonsyndromic cleft lip and palate: evidence of linkage to a microsatellite marker on 6p23. Am. J. Hum. Genet., 56, 337-339.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 337-339
-
-
Carinci, F.1
Pezzetti, F.2
Scapoli, L.3
Padula, E.4
Baciliero, U.5
Curioni, C.6
Tognon, M.7
-
19
-
-
0031571130
-
Evidence of linkage to 6p23 and genetic heterogeneity in nonsyndromic cleft lip with or without cleft palate
-
Scapoli, L., Pezzetti, F., Carinci, F., Martinelli, M., Carinci, P. and Tognon, M. (1997) Evidence of linkage to 6p23 and genetic heterogeneity in nonsyndromic cleft lip with or without cleft palate. Genomics, 43, 216-220.
-
(1997)
Genomics
, vol.43
, pp. 216-220
-
-
Scapoli, L.1
Pezzetti, F.2
Carinci, F.3
Martinelli, M.4
Carinci, P.5
Tognon, M.6
-
20
-
-
0032526776
-
A locus in 2p13-p14 (OFC2), in addition to that mapped in 6p23, is involved in nonsyndromic familial orofacial cleft malformation
-
Pezzetti, F., Scapoli, L., Martinelli, M., Carinci, F., Bodo, M., Carinci, P. and Tognon, M. (1998) A locus in 2p13-p14 (OFC2), in addition to that mapped in 6p23, is involved in nonsyndromic familial orofacial cleft malformation. Genomics, 50, 299-305.
-
(1998)
Genomics
, vol.50
, pp. 299-305
-
-
Pezzetti, F.1
Scapoli, L.2
Martinelli, M.3
Carinci, F.4
Bodo, M.5
Carinci, P.6
Tognon, M.7
-
21
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N. and Merikangas, K. (1996) The future of genetic studies of complex human diseases. Science, 273, 1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
22
-
-
0023694945
-
Palate development
-
Ferguson, M.J.W. (1988) Palate development. Development, 103, 41-60.
-
(1988)
Development
, vol.103
, pp. 41-60
-
-
Ferguson, M.J.W.1
-
23
-
-
0024432231
-
Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate
-
Ardinger, H.H., Buetow, K.H., Bell, G.I., Bardach, J., VanDemark, D.R. and Murray, J.C. (1989) Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate. Am. J. Hum. Genet., 45, 348-353.
-
(1989)
Am. J. Hum. Genet.
, vol.45
, pp. 348-353
-
-
Ardinger, H.H.1
Buetow, K.H.2
Bell, G.I.3
Bardach, J.4
Vandemark, D.R.5
Murray, J.C.6
-
24
-
-
0030993005
-
Transforming growth factor alpha locus and nonsyndromic cleft lip with or without cleft palate: A reappraisal
-
Mitchell, L.E. (1997) Transforming growth factor alpha locus and nonsyndromic cleft lip with or without cleft palate: a reappraisal. Genet. Epidemiol., 14, 231-240.
-
(1997)
Genet. Epidemiol.
, vol.14
, pp. 231-240
-
-
Mitchell, L.E.1
-
25
-
-
0028970498
-
Evidence for an association between nonsyndromic cleft lip with or without cleft palate and a gene located on the long arm of chromosome 4
-
Mitchell, L.E., Healey, S.C. and Chenevix-Trench, G. (1995) Evidence for an association between nonsyndromic cleft lip with or without cleft palate and a gene located on the long arm of chromosome 4. Am. J. Hum. Genet., 57, 1130-1136.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 1130-1136
-
-
Mitchell, L.E.1
Healey, S.C.2
Chenevix-Trench, G.3
-
26
-
-
0032231873
-
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans
-
Lidral, A.C., Romitti, P.A., Basart, A.M., Doetschman, T., Leysens, N.J., Daack-Hirsch, S., Semina, E.V., Johnson, L.R., Machida, J., Burds, A., Parnell, T.J., Rubenstein, J.L. and Murray, J.C. (1998) Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. Am. J. Hum. Genet., 63, 557-568.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 557-568
-
-
Lidral, A.C.1
Romitti, P.A.2
Basart, A.M.3
Doetschman, T.4
Leysens, N.J.5
Daack-Hirsch, S.6
Semina, E.V.7
Johnson, L.R.8
Machida, J.9
Burds, A.10
Parnell, T.J.11
Rubenstein, J.L.12
Murray, J.C.13
-
27
-
-
0026620226
-
Cleft lip with or without cleft palate: Associations with transforming growth factor alpha and retinoic acid receptor loci
-
Chenevix-Trench, G., Jones, K., Green, A.C., Duffy, D.L. and Martin, N.G. (1992) Cleft lip with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor loci. Am. J. Hum, Genet., 51, 1377-1385.
-
(1992)
Am. J. Hum, Genet.
, vol.51
, pp. 1377-1385
-
-
Chenevix-Trench, G.1
Jones, K.2
Green, A.C.3
Duffy, D.L.4
Martin, N.G.5
-
28
-
-
0030671069
-
Application of transmission disequilibrium lests to nonsyndromic oral clefts: Including candidate genes and environmental exposures in the models
-
Maestri, N.E., Beaty, T.H., Hetmanski, J., Smith, E.A., McIntosh, I., Wyszynski, D.F., Liang, K.Y., Duffy, D.L. and VanderKolk, C. (1997) Application of transmission disequilibrium lests to nonsyndromic oral clefts: including candidate genes and environmental exposures in the models. Am. J. Med. Genet., 73, 337-344.
-
(1997)
Am. J. Med. Genet.
, vol.73
, pp. 337-344
-
-
Maestri, N.E.1
Beaty, T.H.2
Hetmanski, J.3
Smith, E.A.4
McIntosh, I.5
Wyszynski, D.F.6
Liang, K.Y.7
Duffy, D.L.8
Vanderkolk, C.9
-
29
-
-
0029079365
-
Nonsyndromic cleft lip with or without cleft palate: Evidence of linkage to BCL3 in 17 multigenerational families
-
Stein, J., Mulliken, J.B., Stal, S., Gasser, D.L., Malcolm, S., Winter, R., Blanton, S.H., Amos, C., Seemanova, E. and Hecht, J.T. (1995) Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. Am. J. Hum. Genet., 57, 257-272.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 257-272
-
-
Stein, J.1
Mulliken, J.B.2
Stal, S.3
Gasser, D.L.4
Malcolm, S.5
Winter, R.6
Blanton, S.H.7
Amos, C.8
Seemanova, E.9
Hecht, J.T.10
-
30
-
-
0029240543
-
The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11
-
Juriloff, D.M. and Mah, D.G. (1995) The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11. Mamm. Genome, 6, 63-69.
-
(1995)
Mamm. Genome
, vol.6
, pp. 63-69
-
-
Juriloff, D.M.1
Mah, D.G.2
-
31
-
-
0028962438
-
Genetic analysis of the construction of the AEJ.A congenic strain indicates that nonsyndromic CL (P) in the mouse is caused by two loci with epistatic interaction
-
Juriloff, D.M. (1995) Genetic analysis of the construction of the AEJ.A congenic strain indicates that nonsyndromic CL (P) in the mouse is caused by two loci with epistatic interaction. J. Craniofac. Genet. Dev. Biol., 15, 1-12.
-
(1995)
J. Craniofac. Genet. Dev. Biol.
, vol.15
, pp. 1-12
-
-
Juriloff, D.M.1
-
32
-
-
0031000206
-
Genome scan for teratogen-induced clefting susceptibility loci in the mouse: Evidence of both allelic and locus heterogeneity distinguishing cleft lip and cleft palate
-
Diehl, S.R. and Erickson, R.P. (1997) Genome scan for teratogen-induced clefting susceptibility loci in the mouse: evidence of both allelic and locus heterogeneity distinguishing cleft lip and cleft palate. Proc. Natl Acad. Sci. USA, 94, 5231-5236.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 5231-5236
-
-
Diehl, S.R.1
Erickson, R.P.2
-
33
-
-
0028292605
-
Msxl deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
-
Satokata, I. and Maas, R. (1994) Msxl deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nature Genet., 6, 348-356.
-
(1994)
Nature Genet.
, vol.6
, pp. 348-356
-
-
Satokata, I.1
Maas, R.2
-
34
-
-
0031193368
-
Insertional mutation of the mouse Msxl homeobox gene by an nlacZ reporter gene
-
Houzelstein, D., Cohen, A., Buckingham, M.E. and Robert, B. (1997) Insertional mutation of the mouse Msxl homeobox gene by an nlacZ reporter gene. Mech. Dev., 65, 123-133.
-
(1997)
Mech. Dev.
, vol.65
, pp. 123-133
-
-
Houzelstein, D.1
Cohen, A.2
Buckingham, M.E.3
Robert, B.4
-
35
-
-
0000609255
-
Msh-like genes: A family of homeobox genes with wide-ranging expression during vertebrate development
-
Davidson, D.R. and Hill, R.E. (1991) Msh-like genes: a family of homeobox genes with wide-ranging expression during vertebrate development. Semin. Dev. Biol., 2, 405-412.
-
(1991)
Semin. Dev. Biol.
, vol.2
, pp. 405-412
-
-
Davidson, D.R.1
Hill, R.E.2
-
36
-
-
0028972869
-
Transforming growth factor-beta 3 is required for secondary palate fusion
-
Proetzel, G., Pawlowski, S.A., Wiles, M.V., Yin, M., Boivin, G.P., Howles, P.N., Ding, J., Ferguson, M.W. and Doetschman, T. (1995) Transforming growth factor-beta 3 is required for secondary palate fusion. Nature Genet., 11, 409-414.
-
(1995)
Nature Genet.
, vol.11
, pp. 409-414
-
-
Proetzel, G.1
Pawlowski, S.A.2
Wiles, M.V.3
Yin, M.4
Boivin, G.P.5
Howles, P.N.6
Ding, J.7
Ferguson, M.W.8
Doetschman, T.9
-
37
-
-
0028806184
-
Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction
-
Kaartinen, V., Voncken, J.W., Shuler, C., Warburton, D., Bu, D., Heisterkamp, N. and Groffen, J. (1995) Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction. Nature Genet., 11, 415-421.
-
(1995)
Nature Genet.
, vol.11
, pp. 415-421
-
-
Kaartinen, V.1
Voncken, J.W.2
Shuler, C.3
Warburton, D.4
Bu, D.5
Heisterkamp, N.6
Groffen, J.7
-
38
-
-
0025287681
-
Differential expression of TGF beta isoforms in murine palatogenesis
-
Fitzpatrick, D.R., Denhez, F., Kondaiah, P. and Akhurst, R.J. (1990) Differential expression of TGF beta isoforms in murine palatogenesis. Development, 109, 585-595.
-
(1990)
Development
, vol.109
, pp. 585-595
-
-
Fitzpatrick, D.R.1
Denhez, F.2
Kondaiah, P.3
Akhurst, R.J.4
-
39
-
-
0030953268
-
Transforming growth factor-beta3 regulates transdifferentiation of medial edge epithelium during palatal fusion and associated degradation of the basement membrane
-
Kaartinen, V., Cui, X.M., Heisterkamp, N., Groffen, J. and Shuler, C.F. (1997) Transforming growth factor-beta3 regulates transdifferentiation of medial edge epithelium during palatal fusion and associated degradation of the basement membrane. Dev. Dyn., 209, 255-260.
-
(1997)
Dev. Dyn.
, vol.209
, pp. 255-260
-
-
Kaartinen, V.1
Cui, X.M.2
Heisterkamp, N.3
Groffen, J.4
Shuler, C.F.5
-
40
-
-
0031594269
-
TGFbeta3 promotes transformation of chicken palate medial edge epithelium to mesenchyme in vitro
-
Sun, D., Vanderburg, C.R., Odierna, G.S. and Hay, E.D. (1998) TGFbeta3 promotes transformation of chicken palate medial edge epithelium to mesenchyme in vitro. Development, 125, 95-105.
-
(1998)
Development
, vol.125
, pp. 95-105
-
-
Sun, D.1
Vanderburg, C.R.2
Odierna, G.S.3
Hay, E.D.4
-
41
-
-
0029932086
-
Transcription factor AP-2 essential for cranial closure and craniofacial development
-
Schorle, H., Meier, P., Buchen, M., Jaenisch, R. and Mitchell, P.J. (1996) Transcription factor AP-2 essential for cranial closure and craniofacial development. Nature, 381, 235-238.
-
(1996)
Nature
, vol.381
, pp. 235-238
-
-
Schorle, H.1
Meier, P.2
Buchen, M.3
Jaenisch, R.4
Mitchell, P.J.5
-
42
-
-
0032506118
-
AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice
-
Nottoli, T., Hagopian-Donaldson, S., Zhang, J., Perkins, A. and Williams, T. (1998) AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice. Proc. Natl Acad. Sci. USA, 95, 13714-13719.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 13714-13719
-
-
Nottoli, T.1
Hagopian-Donaldson, S.2
Zhang, J.3
Perkins, A.4
Williams, T.5
-
43
-
-
0026849641
-
Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3
-
Donnai, D., Heather, L.J., Sinclair, P., Thakker, Y., Scambler, P.J. and Dixon, M.J. (1992) Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3. Clin. Dysmorphol., 1, 89-97.
-
(1992)
Clin. Dysmorphol.
, vol.1
, pp. 89-97
-
-
Donnai, D.1
Heather, L.J.2
Sinclair, P.3
Thakker, Y.4
Scambler, P.J.5
Dixon, M.J.6
-
44
-
-
0031658337
-
Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting
-
Davies, A.F., Imaizumi, K., Mirza, G., Stephens, R.S., Kuroki, Y., Matsuno, M. and Ragoussis, J. (1998) Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting. J. Med. Genet., 35, 857-861.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 857-861
-
-
Davies, A.F.1
Imaizumi, K.2
Mirza, G.3
Stephens, R.S.4
Kuroki, Y.5
Matsuno, M.6
Ragoussis, J.7
-
45
-
-
0023275513
-
Linkage of an X-chromosome cleft palate gene
-
Moore, G.E., Ivens, A., Chambers, J., Farrall, M., Williamson, R., Page, D.C., Bjornsson, A., Arnason, A. and Jensson, O. (1987) Linkage of an X-chromosome cleft palate gene. Nature, 326, 91-92.
-
(1987)
Nature
, vol.326
, pp. 91-92
-
-
Moore, G.E.1
Ivens, A.2
Chambers, J.3
Farrall, M.4
Williamson, R.5
Page, D.C.6
Bjornsson, A.7
Arnason, A.8
Jensson, O.9
-
46
-
-
0030064383
-
Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3
-
Forbes, S.A., Brennan, L., Richardson, M., Coffey, A., Cole, C.G., Gregory, S.G., Bentley, D.R., Mumm, S., Moore, G.E. and Stanier, P. (1996) Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3. Genomics, 31, 36-43.
-
(1996)
Genomics
, vol.31
, pp. 36-43
-
-
Forbes, S.A.1
Brennan, L.2
Richardson, M.3
Coffey, A.4
Cole, C.G.5
Gregory, S.G.6
Bentley, D.R.7
Mumm, S.8
Moore, G.E.9
Stanier, P.10
-
47
-
-
84920239533
-
Fistula labii inferioris congenita and its association with cleft lip and palate
-
Van der Woude, A. (1954) Fistula labii inferioris congenita and its association with cleft lip and palate. Am. J. Hum. Genet., 6, 244-256.
-
(1954)
Am. J. Hum. Genet.
, vol.6
, pp. 244-256
-
-
Van Der Woude, A.1
-
48
-
-
0342505913
-
Undescribed malformation of the lower lip occurring in four members of one family
-
Murray, J.J. (1860) Undescribed malformation of the lower lip occurring in four members of one family. Pract. Med. Surg., 26, 502-509.
-
(1860)
Pract. Med. Surg.
, vol.26
, pp. 502-509
-
-
Murray, J.J.1
-
49
-
-
0021864620
-
Genetic analysis in families with van der Woude syndrome
-
Burdick, A.B., Bixler, D. and Puckett, C.L. (1985) Genetic analysis in families with van der Woude syndrome. J. Craniofac. Genet. Dev. Biol., 5, 181-208.
-
(1985)
J. Craniofac. Genet. Dev. Biol.
, vol.5
, pp. 181-208
-
-
Burdick, A.B.1
Bixler, D.2
Puckett, C.L.3
-
50
-
-
0023094796
-
Linkage studies in a pedigree with Van der Woude syndrome
-
Wienker, T.F., Hudek, G., Bissbort, S., Mayerova, A., Mauff, G. and Bender, K. (1987) Linkage studies in a pedigree with Van der Woude syndrome. J. Med. Genet., 24, 160-162.
-
(1987)
J. Med. Genet.
, vol.24
, pp. 160-162
-
-
Wienker, T.F.1
Hudek, G.2
Bissbort, S.3
Mayerova, A.4
Mauff, G.5
Bender, K.6
-
51
-
-
0022873835
-
Lip pits and deletion Iq32-41
-
Bocian, M. and Walker, A.P. (1987) Lip pits and deletion Iq32-41. Am. J. Med. Genet., 26, 437-443.
-
(1987)
Am. J. Med. Genet.
, vol.26
, pp. 437-443
-
-
Bocian, M.1
Walker, A.P.2
-
52
-
-
11944262571
-
Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome 1q
-
Murray, J.C., Nishimura, D.Y., Buetow, K.H., Ardinger, H.H., Spence, M.A., Sparkes, R.S., Falk, R.E., Falk, P.M., Gardner, R.J., Harkness, E.M. et al. (1990) Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome 1q. Am. J. Hum. Genet., 46, 486-491.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 486-491
-
-
Murray, J.C.1
Nishimura, D.Y.2
Buetow, K.H.3
Ardinger, H.H.4
Spence, M.A.5
Sparkes, R.S.6
Falk, R.E.7
Falk, P.M.8
Gardner, R.J.9
Harkness, E.M.10
-
53
-
-
0028896076
-
Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414
-
Sander, A., Murray, J.C., Scherpbier-Heddema, T., Buetow, K.H., Weissenbach, J., Zingg, M., Ludwig, K. and Schmelzle, R. (1995) Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414. Am. J. Hum. Genet., 56, 310-318.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 310-318
-
-
Sander, A.1
Murray, J.C.2
Scherpbier-Heddema, T.3
Buetow, K.H.4
Weissenbach, J.5
Zingg, M.6
Ludwig, K.7
Schmelzle, R.8
-
54
-
-
0030587440
-
Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41
-
Schutte, B.C., Sander, A., Malik, M. and Murray, J.C. (1996) Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41. Genomics, 36, 507-514.
-
(1996)
Genomics
, vol.36
, pp. 507-514
-
-
Schutte, B.C.1
Sander, A.2
Malik, M.3
Murray, J.C.4
-
55
-
-
0028293311
-
Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome
-
Sander, A., Schmelzle, R. and Murray, J. (1994) Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome. Hum. Mol. Genet., 3, 575-578.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 575-578
-
-
Sander, A.1
Schmelzle, R.2
Murray, J.3
-
56
-
-
0032903763
-
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome
-
Schutte, B.C., Basart, A.M., Watanabe, Y., Laffin, J.J., Coppage, K., Bjork, B.C., Daack-Hirsch, S., Patil, S., Dixon, M.J. and Murray, J.C. (1999) Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome. Am. J. Med. Genet., 84, 145-150.
-
(1999)
Am. J. Med. Genet.
, vol.84
, pp. 145-150
-
-
Schutte, B.C.1
Basart, A.M.2
Watanabe, Y.3
Laffin, J.J.4
Coppage, K.5
Bjork, B.C.6
Daack-Hirsch, S.7
Patil, S.8
Dixon, M.J.9
Murray, J.C.10
-
57
-
-
0012524297
-
Congenital malformations induced in rats by maternal nutritional deficiency
-
Warkany, J., Nelson, R.C. and Schraffenberger, E. (1943) Congenital malformations induced in rats by maternal nutritional deficiency. Am. J. Dis. Child., 65, 882-894.
-
(1943)
Am. J. Dis. Child.
, vol.65
, pp. 882-894
-
-
Warkany, J.1
Nelson, R.C.2
Schraffenberger, E.3
-
58
-
-
0029758424
-
Review of the role of potential teratogens in the origin of human nonsyndromic oral clefts
-
Wyszynski, D.F. and Beaty, T.H. (1996) Review of the role of potential teratogens in the origin of human nonsyndromic oral clefts. Teratology, 53, 309-317.
-
(1996)
Teratology
, vol.53
, pp. 309-317
-
-
Wyszynski, D.F.1
Beaty, T.H.2
-
59
-
-
0032906780
-
Parental agricultural work and selected congenital malformations
-
Garcia, A.M., Fletcher, T., Benavides, F.G. and Orts, E. (1999) Parental agricultural work and selected congenital malformations. Am. J. Epidemiol., 149, 64-74.
-
(1999)
Am. J. Epidemiol.
, vol.149
, pp. 64-74
-
-
Garcia, A.M.1
Fletcher, T.2
Benavides, F.G.3
Orts, E.4
-
60
-
-
0012610212
-
Familial risk of recurrence of clefts of the lip and palate
-
Cembrano, J.R.J., Vera, J.S.d., Joaquino, J.B., Ng, E.F., Tongson, T.L., Manalo, P.D., Fernandez, G.C. and Encarnacion, R.C. (1995) Familial risk of recurrence of clefts of the lip and palate. Philipp. J. Surg. Surg. Spec., 50, 37-40.
-
(1995)
Philipp. J. Surg. Surg. Spec.
, vol.50
, pp. 37-40
-
-
Cembrano, J.R.J.1
Vera, J.S.D.2
Joaquino, J.B.3
Ng, E.F.4
Tongson, T.L.5
Manalo, P.D.6
Fernandez, G.C.7
Encarnacion, R.C.8
-
62
-
-
0023608443
-
Genetic epidemiology of cleft lip with or without cleft palate in the population of Hawaii
-
Chung, C.S., Mi, M.P. and Beechert, A.M. (1987) Genetic epidemiology of cleft lip with or without cleft palate in the population of Hawaii. Genet. Epidemiol., 4, 415-423.
-
(1987)
Genet. Epidemiol.
, vol.4
, pp. 415-423
-
-
Chung, C.S.1
Mi, M.P.2
Beechert, A.M.3
-
63
-
-
0030596975
-
Gentagelsesrisiko for laebe-ganespalte efter partner- Eller adresseskift
-
Christensen, K., Schmidt, M.M., Vaeth, M. and Olsen, J. (1996) Gentagelsesrisiko for laebe-ganespalte efter partner- eller adresseskift [Risk of the recurrence of cleft lip and palate after changing of partner or residence]. Ugeskr. Laeger, 158, 6103-6106.
-
(1996)
Ugeskr. Laeger
, vol.158
, pp. 6103-6106
-
-
Christensen, K.1
Schmidt, M.M.2
Vaeth, M.3
Olsen, J.4
-
64
-
-
0030696738
-
Evolving methods in genetic epidemiology. III. Gene-environment interaction in epidemiologic research
-
Yang, Q. and Khoury, M.J. (1997) Evolving methods in genetic epidemiology. III. Gene-environment interaction in epidemiologic research. Epidemiol. Rev., 19, 33-43.
-
(1997)
Epidemiol. Rev.
, vol.19
, pp. 33-43
-
-
Yang, Q.1
Khoury, M.J.2
-
65
-
-
0029053191
-
Absence of an environmental effect on the recurrence of facial-cleft defects
-
Christensen, K., Schmidt, M.M., Vaeth, M. and Olsen, J. (1995) Absence of an environmental effect on the recurrence of facial-cleft defects. N. Engl. J. Med., 333, 161-164.
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 161-164
-
-
Christensen, K.1
Schmidt, M.M.2
Vaeth, M.3
Olsen, J.4
-
66
-
-
9844229072
-
Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996
-
Beaty, T.H., Maestri, N.E., Hetmanski, J.B., Wyszynski, D.F., Vanderkolk, C.A., Simpson, J.C., McIntosh, I., Smith, E.A., Zeiger, J.S., Raymond, G.V., Panny, S.R., Tifft, C.J., Lewanda, A.F., Cristion, C.A. and Wulfsberg, E.A. (1997) Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996. Cleft Palate Craniofac. J., 34, 447-454.
-
(1997)
Cleft Palate Craniofac. J.
, vol.34
, pp. 447-454
-
-
Beaty, T.H.1
Maestri, N.E.2
Hetmanski, J.B.3
Wyszynski, D.F.4
Vanderkolk, C.A.5
Simpson, J.C.6
McIntosh, I.7
Smith, E.A.8
Zeiger, J.S.9
Raymond, G.V.10
Panny, S.R.11
Tifft, C.J.12
Lewanda, A.F.13
Cristion, C.A.14
Wulfsberg, E.A.15
-
67
-
-
0030029864
-
Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants
-
Shaw, G.M., Wasserman, C.R., Lammer, E.J., O'Malley, C.D., Murray, J.C., Basart, A.M. and Tolarova, M.M. (1996) Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants. Am. J. Hum. Genet., 58, 551-561.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 551-561
-
-
Shaw, G.M.1
Wasserman, C.R.2
Lammer, E.J.3
O'Malley, C.D.4
Murray, J.C.5
Basart, A.M.6
Tolarova, M.M.7
-
68
-
-
0031815048
-
Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use
-
Shaw, G.M., Wasserman, C.R., Murray, J.C. and Lammer, E.J. (1998) Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use. Cleft Palate Craniofac. J., 35, 366-370.
-
(1998)
Cleft Palate Craniofac. J.
, vol.35
, pp. 366-370
-
-
Shaw, G.M.1
Wasserman, C.R.2
Murray, J.C.3
Lammer, E.J.4
-
69
-
-
0033081772
-
Oral clefts, transforming growth factor alpha gene variants, and maternal smoking: A population-based case-control study in Denmark, 1991-1994
-
Christensen, K., Olsen, J., Norgaard-Pedersen, B., Basso, O., Stovring, H., Milhollin-Johnson, L. and Murray, J.C. (1999) Oral clefts, transforming growth factor alpha gene variants, and maternal smoking: a population-based case-control study in Denmark, 1991-1994. Am. J. Epidemiol., 149, 248-255.
-
(1999)
Am. J. Epidemiol.
, vol.149
, pp. 248-255
-
-
Christensen, K.1
Olsen, J.2
Norgaard-Pedersen, B.3
Basso, O.4
Stovring, H.5
Milhollin-Johnson, L.6
Murray, J.C.7
-
70
-
-
0032989710
-
Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: Evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts
-
Romitti, P.A., Lidral, A.C., Munger, R.G., Daack-Hirsch, S., Burns, T.L. and Murray, J.C. (1999) Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts. Teratology, 59, 39-50.
-
(1999)
Teratology
, vol.59
, pp. 39-50
-
-
Romitti, P.A.1
Lidral, A.C.2
Munger, R.G.3
Daack-Hirsch, S.4
Burns, T.L.5
Murray, J.C.6
-
71
-
-
0029854517
-
Maternal alcohol use and risk of orofacial cleft birth defects
-
Munger, R.G., Romitli, P.A., Daack-Hirsch, S., Burns, T.L., Murray, J.C. and Hanson, J. (1996) Maternal alcohol use and risk of orofacial cleft birth defects. Teratology, 54, 27-33.
-
(1996)
Teratology
, vol.54
, pp. 27-33
-
-
Munger, R.G.1
Romitli, P.A.2
Daack-Hirsch, S.3
Burns, T.L.4
Murray, J.C.5
Hanson, J.6
-
72
-
-
0033506695
-
Maternal periconceptional alcohol consumption and risk for orofacial clefts
-
Shaw, G.M. and Lammer, E.J. (1999) Maternal periconceptional alcohol consumption and risk for orofacial clefts. J. Pediatr., 134, 298-303.
-
(1999)
J. Pediatr.
, vol.134
, pp. 298-303
-
-
Shaw, G.M.1
Lammer, E.J.2
-
73
-
-
0022260109
-
Retinoic acid embryopathy
-
Lammer, E.J., Chen, D.T., Hoar, R.M., Agnish, N.D., Benke, P.J., Braun, J.T., Curry, C.J., Fernhoff, P.M., Grix, A.W.Jr, Lott, I.T. et al. (1985) Retinoic acid embryopathy. N. Engl. J. Med., 313, 837-841.
-
(1985)
N. Engl. J. Med.
, vol.313
, pp. 837-841
-
-
Lammer, E.J.1
Chen, D.T.2
Hoar, R.M.3
Agnish, N.D.4
Benke, P.J.5
Braun, J.T.6
Curry, C.J.7
Fernhoff, P.M.8
Grix A.W., Jr.9
Lott, I.T.10
-
74
-
-
0029022223
-
Reduced recurrence of orofacial clefts after periconceptional supplementation with high-dose folic acid and multivitamins
-
Tolarova, M. and Harris, J. (1995) Reduced recurrence of orofacial clefts after periconceptional supplementation with high-dose folic acid and multivitamins. Teratology, 51, 71-78.
-
(1995)
Teratology
, vol.51
, pp. 71-78
-
-
Tolarova, M.1
Harris, J.2
-
75
-
-
0030628493
-
Orofacial clefts in Hungary. Epidemiological and genetic data, primary prevention
-
Creizel, A.E. and Hirschberg, J. (1997) Orofacial clefts in Hungary. Epidemiological and genetic data, primary prevention. Folia Phoniatr. Logop., 49, 111-116.
-
(1997)
Folia Phoniatr. Logop.
, vol.49
, pp. 111-116
-
-
Creizel, A.E.1
Hirschberg, J.2
-
76
-
-
0029893565
-
Case-control study of periconceptional folic acid supplementation and oral clefts
-
Hayes, C., Werler, M.M., Willett, W.C. and Mitchell, A.A. (1996) Case-control study of periconceptional folic acid supplementation and oral clefts. Am. J. Epidemiol., 143, 1229-1234.
-
(1996)
Am. J. Epidemiol.
, vol.143
, pp. 1229-1234
-
-
Hayes, C.1
Werler, M.M.2
Willett, W.C.3
Mitchell, A.A.4
-
77
-
-
0031785528
-
Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip
-
Shaw, G.M., Rozen, R., Finnell, R.H., Todoroff, K. and Lammer, E.J. (1998) Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip. Am. J. Med. Genet., 80, 196-198.
-
(1998)
Am. J. Med. Genet.
, vol.80
, pp. 196-198
-
-
Shaw, G.M.1
Rozen, R.2
Finnell, R.H.3
Todoroff, K.4
Lammer, E.J.5
-
78
-
-
0030615238
-
Effects of vitamin B6 on beta-aminoproprionitrile-induced palatal cleft formation in the rat
-
Jacobsson, C. and Granstrom, G. (1997) Effects of vitamin B6 on beta-aminoproprionitrile-induced palatal cleft formation in the rat. Cleft Palate Craniofac. J., 34, 95-100.
-
(1997)
Cleft Palate Craniofac. J.
, vol.34
, pp. 95-100
-
-
Jacobsson, C.1
Granstrom, G.2
-
79
-
-
0028023622
-
Bendectin and birth detects: I. A meta-analysis of the epidemiologic studies
-
McKeigue, P.M., Lamm, S.H., Linn, S. and Kutcher, J.S. (1994) Bendectin and birth detects: I. A meta-analysis of the epidemiologic studies. Teratology, 50, 27-37.
-
(1994)
Teratology
, vol.50
, pp. 27-37
-
-
McKeigue, P.M.1
Lamm, S.H.2
Linn, S.3
Kutcher, J.S.4
-
80
-
-
0032540271
-
Endocrine disruptors signal the need for receptor models and mechanisms to inform policy
-
Limbird, L.E. and Taylor, P. (1998) Endocrine disruptors signal the need for receptor models and mechanisms to inform policy. Cell, 93, 157-163.
-
(1998)
Cell
, vol.93
, pp. 157-163
-
-
Limbird, L.E.1
Taylor, P.2
-
81
-
-
0032030839
-
Control of cell lineage-specific development and transcription by bHLH-PAS proteins
-
Crews, S.T. (1998) Control of cell lineage-specific development and transcription by bHLH-PAS proteins. Genes Dev., 12, 607-620.
-
(1998)
Genes Dev.
, vol.12
, pp. 607-620
-
-
Crews, S.T.1
-
82
-
-
0031971047
-
Expression of ARNT, ARNT2, HIFI alpha, HIF2 alpha and Ah receptor mRNAs in the developing mouse
-
Jain, S., Maltepe, E., Lu, M.M., Simon, C. and Bradfield, C.A. (1998) Expression of ARNT, ARNT2, HIFI alpha, HIF2 alpha and Ah receptor mRNAs in the developing mouse. Mech. Dev., 73, 117-123.
-
(1998)
Mech. Dev.
, vol.73
, pp. 117-123
-
-
Jain, S.1
Maltepe, E.2
Lu, M.M.3
Simon, C.4
Bradfield, C.A.5
-
83
-
-
0031693559
-
AH receptor, ARNT, glucocorticoid receptor, EGF receptor, EGF, TGF alpha, TGF beta 1, TGF beta 2, and TGF beta 3 expression in human embryonic palate, and effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)
-
Abbott, B.D., Probst, M.R., Perdew, G.H. and Buckalew, A.R. (1998) AH receptor, ARNT, glucocorticoid receptor, EGF receptor, EGF, TGF alpha, TGF beta 1, TGF beta 2, and TGF beta 3 expression in human embryonic palate, and effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Teratology, 58, 30-43.
-
(1998)
Teratology
, vol.58
, pp. 30-43
-
-
Abbott, B.D.1
Probst, M.R.2
Perdew, G.H.3
Buckalew, A.R.4
-
84
-
-
0031694284
-
Differential expression and biological activity of retinoic acid-induced TGFbeta isoforms in embryonic palate mesenchymal cells
-
Nugent, P., Ma, L. and Greene, R.M. (1998) Differential expression and biological activity of retinoic acid-induced TGFbeta isoforms in embryonic palate mesenchymal cells. J. Cell. Physiol., 177, 36-46.
-
(1998)
J. Cell. Physiol.
, vol.177
, pp. 36-46
-
-
Nugent, P.1
Ma, L.2
Greene, R.M.3
-
85
-
-
7144242310
-
Mesenchymal changes associated with retinoic acid induced cleft palate in CD-1 mice
-
Degitz, S.J., Francis, B.M. and Foley, G.L. (1998) Mesenchymal changes associated with retinoic acid induced cleft palate in CD-1 mice. J. Craniofac. Genet. Dev. Biol. 18, 88-99.
-
(1998)
J. Craniofac. Genet. Dev. Biol.
, vol.18
, pp. 88-99
-
-
Degitz, S.J.1
Francis, B.M.2
Foley, G.L.3
-
86
-
-
0030093934
-
Comparative teratological studies on TCDD, endrin and lindane in C57BL/6J and DBA/2J mice
-
Hassoun, E.A. and Stohs, S.J. (1996) Comparative teratological studies on TCDD, endrin and lindane in C57BL/6J and DBA/2J mice. Comp. Biochem. Physiol., 113C, 393-398.
-
(1996)
Comp. Biochem. Physiol.
, vol.113 C
, pp. 393-398
-
-
Hassoun, E.A.1
Stohs, S.J.2
-
87
-
-
0031773906
-
Role of TGF-beta in RA-induced cleft palate in CD-1 mice
-
Degitz, S.J., Morris, D., Foley, G.L. and Francis, B.M. (1998) Role of TGF-beta in RA-induced cleft palate in CD-1 mice. Teratology, 58, 197-204.
-
(1998)
Teratology
, vol.58
, pp. 197-204
-
-
Degitz, S.J.1
Morris, D.2
Foley, G.L.3
Francis, B.M.4
-
88
-
-
0028360062
-
Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1
-
Kurihara, Y., Kurihara, H., Suzuki, H., Kodama, T., Maemura, K., Nagai, R., Oda, H., Kuwaki, T., Cao, W.H., Kamada, N. et al. (1994) Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1. Nature, 368, 703-710.
-
(1994)
Nature
, vol.368
, pp. 703-710
-
-
Kurihara, Y.1
Kurihara, H.2
Suzuki, H.3
Kodama, T.4
Maemura, K.5
Nagai, R.6
Oda, H.7
Kuwaki, T.8
Cao, W.H.9
Kamada, N.10
-
89
-
-
0030799236
-
Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial patterning, and skeletal muscle development
-
Berk, M., Desai, S.Y., Heyman, H.C. and Colmenares, C. (1997) Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial patterning, and skeletal muscle development. Genes Dev., 11, 2029-2039.
-
(1997)
Genes Dev.
, vol.11
, pp. 2029-2039
-
-
Berk, M.1
Desai, S.Y.2
Heyman, H.C.3
Colmenares, C.4
-
90
-
-
0030955889
-
Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: Mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches
-
Qiu, M., Bulfone, A., Ghattas, I., Meneses, J.J., Christensen, L., Sharpe, P.T., Presley, R., Pedersen, R.A. and Rubenstein, J.L. (1997) Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches. Dev. Biol., 185, 165-184.
-
(1997)
Dev. Biol.
, vol.185
, pp. 165-184
-
-
Qiu, M.1
Bulfone, A.2
Ghattas, I.3
Meneses, J.J.4
Christensen, L.5
Sharpe, P.T.6
Presley, R.7
Pedersen, R.A.8
Rubenstein, J.L.9
-
91
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
-
Semina, E.V., Reiter, R., Leysens, N.J., Alward, W.L., Small, K.W., Datson, N.A., Siegel-Bartelt, J., Bierke-Nelson, D., Bitoun, P., Zabel, B.U., Carey, J.C. and Murray, J.C. (1996) Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nature Genet., 14, 392-399.
-
(1996)
Nature Genet.
, vol.14
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
Alward, W.L.4
Small, K.W.5
Datson, N.A.6
Siegel-Bartelt, J.7
Bierke-Nelson, D.8
Bitoun, P.9
Zabel, B.U.10
Carey, J.C.11
Murray, J.C.12
-
92
-
-
0032169255
-
Pax9-deficienl mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities
-
Peters, H., Neubuser, A., Kratochwil, K. and Balling, R. (1998) Pax9-deficienl mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. Genes Dev., 12, 2735-2747.
-
(1998)
Genes Dev.
, vol.12
, pp. 2735-2747
-
-
Peters, H.1
Neubuser, A.2
Kratochwil, K.3
Balling, R.4
-
93
-
-
17344366813
-
A mouse model for hereditary thyroid dysgenesis and cleft palate
-
De Felice, M., Ovitt, C., Biffali, E., Rodriguez-Mallon, A., Arra, C., Anastassiadis, K., Macchia, P.E., Mattei, M.G., Mariano, A., Scholer, H., Macchia, V. and Di Lauro, R. (1998) A mouse model for hereditary thyroid dysgenesis and cleft palate. Nature Genet., 19, 395-398.
-
(1998)
Nature Genet.
, vol.19
, pp. 395-398
-
-
De Felice, M.1
Ovitt, C.2
Biffali, E.3
Rodriguez-Mallon, A.4
Arra, C.5
Anastassiadis, K.6
Macchia, P.E.7
Mattei, M.G.8
Mariano, A.9
Scholer, H.10
Macchia, V.11
Di Lauro, R.12
-
94
-
-
0031820442
-
Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
-
Clifton-Bligh, R.J., Wentworth, J.M., Heinz, P., Crisp, M.S., John, R., Lazarus, J.H., Ludgate, M. and Chatterjee, V.K. (1998) Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia. Nature Genet., 19, 399-401.
-
(1998)
Nature Genet.
, vol.19
, pp. 399-401
-
-
Clifton-Bligh, R.J.1
Wentworth, J.M.2
Heinz, P.3
Crisp, M.S.4
John, R.5
Lazarus, J.H.6
Ludgate, M.7
Chatterjee, V.K.8
-
95
-
-
8044231337
-
Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines
-
Lidral, A.C., Murray, J.C., Buetow, K.H., Basart, A.M., Schearer, H., Shiang, R., Naval, A., Layda, E., Magee, K. and Magee, W. (1997) Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines. Cleft Palate Craniofac. J., 34, 1-6.
-
(1997)
Cleft Palate Craniofac. J.
, vol.34
, pp. 1-6
-
-
Lidral, A.C.1
Murray, J.C.2
Buetow, K.H.3
Basart, A.M.4
Schearer, H.5
Shiang, R.6
Naval, A.7
Layda, E.8
Magee, K.9
Magee, W.10
-
96
-
-
0028130047
-
Possible localization of a major gene for cleft lip and palate to 4q
-
Beiraghi, S., Foroud, T., Diouhy, S., Bixler, D., Conneally, P.M., Delozier-Blanchet, D. and Hodes, M.E. (1994) Possible localization of a major gene for cleft lip and palate to 4q. Clin. Genet., 46, 255-256.
-
(1994)
Clin. Genet.
, vol.46
, pp. 255-256
-
-
Beiraghi, S.1
Foroud, T.2
Diouhy, S.3
Bixler, D.4
Conneally, P.M.5
Delozier-Blanchet, D.6
Hodes, M.E.7
-
97
-
-
0027295566
-
Exclusion of candidate genes from a role in cleft lip with or without cleft palate: Linkage and association studies
-
Vintiner, G.M., Lo, K.K., Holder, S.E., Winter, R.M. and Malcolm, S. (1993) Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies. J. Med. Genet., 30, 773-778.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 773-778
-
-
Vintiner, G.M.1
Lo, K.K.2
Holder, S.E.3
Winter, R.M.4
Malcolm, S.5
-
98
-
-
0027358433
-
Further evidence of a relationship between the retinoic acid receptor alpha locus and nonsyndromic cleft lip with or without cleft palate (CL+/- P)
-
Shaw, D., Ray, A., Marazita, M. and Field, L. (1993) Further evidence of a relationship between the retinoic acid receptor alpha locus and nonsyndromic cleft lip with or without cleft palate (CL+/- P). Am. J Hum. Genet., 53, 1156-1157.
-
(1993)
Am. J Hum. Genet.
, vol.53
, pp. 1156-1157
-
-
Shaw, D.1
Ray, A.2
Marazita, M.3
Field, L.4
-
99
-
-
0028242663
-
Interpreting the evidence for an association between the retinoic acid receptor locus and non-syndromic cleft lip with or without cleft palate
-
Mitchell, L.E. (1994) Interpreting the evidence for an association between the retinoic acid receptor locus and non-syndromic cleft lip with or without cleft palate. J. Med. Genet., 31, 425.
-
(1994)
J. Med. Genet.
, vol.31
, pp. 425
-
-
Mitchell, L.E.1
-
100
-
-
0031060648
-
Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families
-
Wyszynski, D.F., Maestri, N., McIntosh, I., Smith, E.A., Lewanda, A.F., Garcia-Delgado, C., Vinageras-Guarneros, E., Wulfsberg, E. and Beaty, T.H. (1997) Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families. Hum. Genet., 99, 22-26.
-
(1997)
Hum. Genet.
, vol.99
, pp. 22-26
-
-
Wyszynski, D.F.1
Maestri, N.2
McIntosh, I.3
Smith, E.A.4
Lewanda, A.F.5
Garcia-Delgado, C.6
Vinageras-Guarneros, E.7
Wulfsberg, E.8
Beaty, T.H.9
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