-
1
-
-
0024432231
-
Association of genetic variation of the transforming growth factoralpha gene with cleft lip and palate
-
Ardinger, H. H., Buetow, K. H., Bell, G. I., Bardach, J., Van Demark, D. R. & Murray, J. G. (1989). Association of genetic variation of the transforming growth factoralpha 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
Van Demark, D.R.5
Murray, J.G.6
-
2
-
-
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. & Hodes, M. E. (1994). Possible localization of a major gene for cleft lip and palate to 4q. Clin. Genel. 46, 255-256.
-
(1994)
Clin. Genel.
, 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
-
3
-
-
0022873835
-
Lip pits and deletion Iq32 → 41
-
Bocian, M. & 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
-
4
-
-
0028797751
-
Nondyndromic 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. & Tognon, M. (1995). Nondyndromic 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
-
5
-
-
0033959922
-
Genetics of the nonsyndromic cleft lip and palate: A review of international studies and data regarding the Italian population
-
Carinci, F., Pezzetti, F., Scapoli, L., Martinelli, M., Carinci, P. & Tognon, M. (2000). Genetics of the nonsyndromic cleft lip and palate: a review of international studies and data regarding the Italian population. Cleft Palate Craniofac. J. 37, 33-40.
-
(2000)
Cleft Palate Craniofac. J.
, vol.37
, pp. 33-40
-
-
Carinci, F.1
Pezzetti, F.2
Scapoli, L.3
Martinelli, M.4
Carinci, P.5
Tognon, M.6
-
6
-
-
0016915488
-
Genetics of common single malformations
-
Carter, C. O. (1976). Genetics of common single malformations. Br. Med. Bull. 32, 21-26.
-
(1976)
Br. Med. Bull.
, vol.32
, pp. 21-26
-
-
Carter, C.O.1
-
7
-
-
0026620226
-
Cleft lip with or without cleft palate: Associations with transforming growth factor alpha and retinoic acid receptor loci
-
Chenevix-Trcnch, G., Jones, K., Green, A. C., Duffy, D. L. & 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-Trcnch, G.1
Jones, K.2
Green, A.C.3
Duffy, D.L.4
Martin, N.G.5
-
8
-
-
0027080461
-
Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation
-
Czeizel, A. E. & Dudas, I. (1992). Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N. Engl. J. Med. 26, 1832-1835.
-
(1992)
N. Engl. J. Med.
, vol.26
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudas, I.2
-
9
-
-
0023764339
-
Translocation (1;22) in a child with bilateral oblique clefts
-
Dasouki, M., Barr, M., Erichson, R. P. & Cox, B. (1988). Translocation (1;22) in a child with bilateral oblique clefts. J. Med. Genet. 25, 427-431.
-
(1988)
J. Med. Genet.
, vol.25
, pp. 427-431
-
-
Dasouki, M.1
Barr, M.2
Erichson, R.P.3
Cox, B.4
-
10
-
-
0028816146
-
Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region
-
Davies, A. F., Stephens, R. J., Olavesen, M. G., Heather, L., Dixon, M. J., Magee, A., Flinter, F. & Ragoussis, J. (1995). Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region. Hum. Mol. Genet. 4, 121-128.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 121-128
-
-
Davies, A.F.1
Stephens, R.J.2
Olavesen, M.G.3
Heather, L.4
Dixon, M.J.5
Magee, A.6
Flinter, F.7
Ragoussis, J.8
-
11
-
-
0023176710
-
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignement to chromosome 6
-
Eiberg, H., Bixler, D., Nielsen, L. S., Conneally, P. M. & Mohr, J. (1987). Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignement 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
-
12
-
-
0026500144
-
Familial recurrencepattern analysis of cleft lip with or without cleft palate
-
Farrall, M. & Holder, S. (1992). Familial recurrencepattern analysis of cleft lip with or without cleft palate. Am. J. Hum Genet. 50, 270-277.
-
(1992)
Am. J. Hum Genet.
, vol.50
, pp. 270-277
-
-
Farrall, M.1
Holder, S.2
-
13
-
-
34547474513
-
The genetics of cleft lip and palate
-
Fraser, F. C. (1970). The genetics of cleft lip and palate. Am. J. Hum. Genet. 49, 674-681.
-
(1970)
Am. J. Hum. Genet.
, vol.49
, pp. 674-681
-
-
Fraser, F.C.1
-
14
-
-
0002033556
-
Evidence for an association between nonsyndromic cleft lip with or without cleft palate and a gene located on the long arm of chromosome 4
-
Healey, S. C., Mitchell, L. E. & Chenevix-Trench, G. (1994). 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. 55 (Suppl.), A47.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, Issue.SUPPL.
-
-
Healey, S.C.1
Mitchell, L.E.2
Chenevix-Trench, G.3
-
15
-
-
85016750763
-
Simple and rapid preparation of samples for PCR
-
(Ed. H. A. Erlich), Stockton Press, New York
-
Higuchi, R. (1989). Simple and rapid preparation of samples for PCR. In: PCE technology. (Ed. H. A. Erlich), pp. 31-38. Stockton Press, New York.
-
(1989)
PCE Technology
, pp. 31-38
-
-
Higuchi, R.1
-
16
-
-
34547482796
-
Transmission/ disequilibrium test (TDT) approach at the van der Woude syndrome (vWS) locus in familial non-syndroinic cleft lip with or without cleft palate (NSCL/P).,4m
-
Houdayer, C., Soupre, V.,-Morgant, G:, Munnich, A., Vazquez, M. P. &.Bahuau, M. (1999). Transmission/ disequilibrium test (TDT) approach at the van der Woude syndrome (vWS) locus in familial non-syndroinic cleft lip with or without cleft palate (NSCL/P).,4m. J. Hum. Genet. 65 (Suppl.), A255.
-
(1999)
J. Hum. Genet.
, vol.65
, Issue.SUPPL.
-
-
Houdayer, C.1
Soupre V-Morgant, G.2
Munnich, A.3
Vazquez, M.P.4
Bahuau, M.5
-
17
-
-
0027419349
-
Region of the mouse genome homologous to human chromosome Iq21 affects facial clefting
-
Karolyi, J. & Erickson, R. P. (1993). Region of the mouse genome homologous to human chromosome Iq21 affects facial clefting. J. Craniofac. Genet. Dev. Biol. 13, 1-5.
-
(1993)
J. Craniofac. Genet. Dev. Biol.
, vol.13
, pp. 1-5
-
-
Karolyi, J.1
Erickson, R.P.2
-
18
-
-
0017889216
-
Terminal deletion of the long arm of chromosome 1 in a malformed newborn
-
Kessel, E., Pfeiffer, R. A., Blanke, W. & Schwarz, J. (1978). Terminal deletion of the long arm of chromosome 1 in a malformed newborn. Hum. Genet. 42, 333-337.
-
(1978)
Hum. Genet.
, vol.42
, pp. 333-337
-
-
Kessel, E.1
Pfeiffer, R.A.2
Blanke, W.3
Schwarz, J.4
-
19
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak, L., Daly, M. J., Reeve-Daly, M. P. & Lander, E. S. (1990). Parametric and nonparametric linkage analysis: a unified multipoint approach. Am. J. Hum. Genet. 58, 1347-1363.
-
(1990)
Am. J. Hum. Genet.
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
20
-
-
0342499587
-
Strategies for multilocus analysis in human
-
Lathrop, G. M., Lalowel, J. M., Julier, C. & Ott, J. (1984). Strategies for multilocus analysis in human. Proc. Nail. Acad. Sci. USA 81, 3443-3444.
-
(1984)
Proc. Nail. Acad. Sci. USA
, vol.81
, pp. 3443-3444
-
-
Lathrop, G.M.1
Lalowel, J.M.2
Julier, C.3
Ott, J.4
-
21
-
-
0021232843
-
Genetic analysis of cleft lip with or without cleft palate in Danish kindreds
-
Marazita, M. L., Spence, M. A. & Melnik, M. (1984). Genetic analysis of cleft lip with or without cleft palate in Danish kindreds. Am. J. Med. Genet. 19, 9-18.
-
(1984)
Am. J. Med. Genet.
, vol.19
, pp. 9-18
-
-
Marazita, M.L.1
Spence, M.A.2
Melnik, M.3
-
22
-
-
0032528105
-
Suggestive linkage between markers on chromosome 19ql3.2 and nonsyndromic orofacial cleft malformation
-
Martinelli, M., Scapoli, L., Pezzetti, F., Carinci, F., Carinci, P., Baciliero, U., Padula, E. & Tognon, M. (1998). Suggestive linkage between markers on chromosome 19ql3.2 and nonsyndromic orofacial cleft malformation. Genomics 51, 177-181.
-
(1998)
Genomics
, vol.51
, pp. 177-181
-
-
Martinelli, M.1
Scapoli, L.2
Pezzetti, F.3
Carinci, F.4
Carinci, P.5
Baciliero, U.6
Padula, E.7
Tognon, M.8
-
23
-
-
0035254496
-
C677T variant form at the MTHFR gene and CL/P: A risk factor for mothers?
-
Martinelli, M., Scapoli, L., Pezzetti, F., Carinci, F., Carinci, P., Stabellini, G., Bisceglia, L., Gombos, F. & Tognon, M. (2001). C677T variant form at the MTHFR gene and CL/P: a risk factor for mothers? Am. J. Med, Genet. 98, 357-300.
-
(2001)
Am. J. Med. Genet.
, vol.98
, pp. 357-1300
-
-
Martinelli, M.1
Scapoli, L.2
Pezzetti, F.3
Carinci, F.4
Carinci, P.5
Stabellini, G.6
Bisceglia, L.7
Gombos, F.8
Tognon, M.9
-
24
-
-
0018909527
-
Cleft +/- Cleft palate: An overview of the literature and an analysis of Danish cases born between 1941 and 1908
-
Melnik, M., Bixler, D., Fogh-Anderson, P. & Conncally, P.M. (1980). Cleft +/- cleft palate: an overview of the literature and an analysis of Danish cases born between 1941 and 1908. Am. J. Med. Genet. 6, 83-97.
-
(1980)
Am. J. Med. Genet.
, vol.6
, pp. 83-97
-
-
Melnik, M.1
Bixler, D.2
Fogh-Anderson, P.3
Conncally, P.M.4
-
25
-
-
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
-
26
-
-
0029050592
-
Face facts: Genes, Environment, and Cleft
-
Murray, J. C. (1995). Face facts: Genes, Environment, and Cleft. Am. J. Hum. Genet. 57, 227-232.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 227-232
-
-
Murray, J.C.1
-
27
-
-
0032526776
-
A locus in 2p1314, 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. & Tognon, M. (1998). A locus in 2p1314, in addition to that mapped in 6p23, is involved in nonsyndromic familial orofacial cleft malformation. Genomics 50, 299-300.
-
(1998)
Genomics
, vol.50
, pp. 299-300
-
-
Pezzetti, F.1
Scapoli, L.2
Martinelli, M.3
Carinci, F.4
Bodo, M.5
Carinci, P.6
Tognon, M.7
-
28
-
-
0033793517
-
Linkage analysis of candidate endothelin pathway genes in nonsyndromic familial orofacial cleft
-
Pezzetti, F., Scapoli, L., Martinelli, M., Carinci, F., Brunelli, G., Carls, P., Palomba, F., Gombos, F., Carinci, P. & Tognon, M. (2000). Linkage analysis of candidate endothelin pathway genes in nonsyndromic familial orofacial cleft. Ann. Hum. Genet. 64, 341-343.
-
(2000)
Ann. Hum. Genet.
, vol.64
, pp. 341-343
-
-
Pezzetti, F.1
Scapoli, L.2
Martinelli, M.3
Carinci, F.4
Brunelli, G.5
Carls, P.6
Palomba, F.7
Gombos, F.8
Carinci, P.9
Tognon, M.10
-
29
-
-
0029004701
-
Lack of linkage of apparently dominant cleft lip (palate) to two candidate chromosomal regions
-
Pierpont, J. W., Storm, A. L., Erickson, R. P., Kohn, B. R., Pettijohn, L. & DePaepe, A. (1995). Lack of linkage of apparently dominant cleft lip (palate) to two candidate chromosomal regions. J. Craniofac. Genet. Dev. Biol. 15, 60-71.
-
(1995)
J. Craniofac. Genet. Dev. Biol.
, vol.15
, pp. 60-71
-
-
Pierpont, J.W.1
Storm, A.L.2
Erickson, R.P.3
Kohn, B.R.4
Pettijohn, L.5
Depaepe, A.6
-
30
-
-
0034033146
-
Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs
-
Prescott, N. J., Lees, M. M., Winter, R. M. & Malcolm, S. (2000). Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs. Hum. Genet. 106, 345-350.
-
(2000)
Hum. Genet.
, vol.106
, pp. 345-350
-
-
Prescott, N.J.1
Lees, M.M.2
Winter, R.M.3
Malcolm, S.4
-
31
-
-
0027365374
-
Nonsyndromic cleft lip with or without cleft palate in West Bengal, India: Evidence for an autosomal major locus
-
Ray, A. K., Field, L. L. & Marazita, M. L. (1993). Nonsyndromic cleft lip with or without cleft palate in West Bengal, India: evidence for an autosomal major locus. Am. J. Hum. Genet. 52, 1000-1011.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 1000-1011
-
-
Ray, A.K.1
Field, L.L.2
Marazita, M.L.3
-
32
-
-
0028293311
-
Evidence for a microdeletion in Iq32-41 involving the gene responsible for Van der Woude syndrome
-
Sander, A., Schmelzte, R. & Murray, J. (1994). Evidence for a microdeletion in Iq32-41 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
Schmelzte, R.2
Murray, J.3
-
33
-
-
0032764326
-
Combined segregation and linkage analysis of Nonsyndromic Orofacial Cleft in two candidate regions
-
Scapoli, G., Collins, A., Martinelli, M., Pezzetti, F., Scapoli, L. & Tognon, M. (1999). Combined segregation and linkage analysis of Nonsyndromic Orofacial Cleft in two candidate regions. Ann.-Hum. Genet. 63, 17-25.
-
(1999)
Ann.-Hum. Genet.
, vol.63
, pp. 17-25
-
-
Scapoli, G.1
Collins, A.2
Martinelli, M.3
Pezzetti, F.4
Scapoli, L.5
Tognon, M.6
-
34
-
-
0031571130
-
Evidence of linkage to 6p23 and genetic heterogeneity in nonsyndromic cleft lip with or without cleft palate (CL ± P)
-
Seapoli, L., Pezzetti, F., Carinci, F., Martinelli, M., Carinci, P. & Tognon, M. (1997). Evidence of linkage to 6p23 and genetic heterogeneity in nonsyndromic cleft lip with or without cleft palate (CL ± P). Genomics 43, 210-220.
-
(1997)
Genomics
, vol.43
, pp. 210-220
-
-
Seapoli, L.1
Pezzetti, F.2
Carinci, F.3
Martinelli, M.4
Carinci, P.5
Tognon, M.6
-
35
-
-
0032903763
-
Microdeletions at chromosome bands Iq32-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. & Murray, J. C. (1999). Microdeletions at chromosome bands Iq32-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
-
36
-
-
0033954225
-
A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at Iq32-q41
-
Schutte, B. C., Bjork, B. C., Coppage, K. B., Malik, M. I., Gregory, S. G., Scott, D. J., Brentzell, L. M., Watanabe, Y., Dixon, M. J. & Murray, J. C. (2000). A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at Iq32-q41. Genome lies. 10, 81-94.
-
(2000)
Genome Lies.
, vol.10
, pp. 81-94
-
-
Schutte, B.C.1
Bjork, B.C.2
Coppage, K.B.3
Malik, M.I.4
Gregory, S.G.5
Scott, D.J.6
Brentzell, L.M.7
Watanabe, Y.8
Dixon, M.J.9
Murray, J.C.10
-
37
-
-
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. & 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, 1150-1157.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 1150-1157
-
-
Shaw, D.1
Ray, A.2
Marazita, M.3
Field, L.4
-
38
-
-
0029151571
-
Risks of orofacial clefts in children born to women using multivitamins containing folic acid periconceptionally
-
Shaw, G. M., Lanimer, E. J., Wasserman, C. R., O'Malley, C. D. & Tolarova M. M. (1995). Risks of orofacial clefts in children born to women using multivitamins containing folic acid periconceptionally. Lancet 346, 393-390.
-
(1995)
Lancet
, vol.346
, pp. 393-1390
-
-
Shaw, G.M.1
Lanimer, E.J.2
Wasserman, C.R.3
O'Malley, C.D.4
Tolarova, M.M.5
-
39
-
-
0029079365
-
Nonsyndromic cleft lip with or without cleft palate: Evidence of linkage to BCL3 in multigenerational families
-
Stein, J., Mulliken, J. B., Stal, S., Gasser, D. L., Malcom, S., Winter, R., Amos, C. & Hecht, J. T. (1995). Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 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
Malcom, S.5
Winter, R.6
Amos, C.7
Hecht, J.T.8
-
40
-
-
0002106809
-
A common mutation in the MTHFR gene is a risk factor for nonsyndromic cleft lip and palate anomalies
-
Tolarova, M. M., Van Rooij, I. A. L. M., Pastor, M., Van der Put, N. M. J., Goldberg, A. C., Hol, F., Capozzi, A., Thomas, C. M.G., Pastor, L., Mosby, T., Ferrari, C., Eskes, T. K. A. B. & Steegers-Theunissen, R. P. M. (1998). A common mutation in the MTHFR gene is a risk factor for nonsyndromic cleft lip and palate anomalies. Am. J. Hum. Genet. 63, A27.
-
(1998)
Am. J. Hum. Genet.
, vol.63
-
-
Tolarova, M.M.1
Van Rooij, I.A.L.M.2
Pastor, M.3
Van Der Put, N.M.J.4
Goldberg, A.C.5
Hol, F.6
Capozzi, A.7
Thomas, C.M.G.8
Pastor, L.9
Mosby, T.10
Ferrari, C.11
Eskes, T.K.A.B.12
Steegers-Theunissen, R.P.M.13
-
41
-
-
0031973930
-
Classification and birth prevalence of orofacial clefts
-
Tolarova, M. M. & Cervenka, J. (1998). Classification and birth prevalence of orofacial clefts. Am. J. Med. Genet. 75, 120-137.
-
(1998)
Am. J. Med. Genet.
, vol.75
, pp. 120-137
-
-
Tolarova, M.M.1
Cervenka, J.2
-
42
-
-
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, 244-252.
-
(1954)
Am. J. Hum. Genet.
, vol.6
, pp. 244-252
-
-
Van Der Woude, A.1
-
43
-
-
0029820276
-
Genetics of nonsyndromic oral clefts revisited
-
Wyszynski, D. F., Beaty, T. H. & Maestri, N. (1990). Genetics of nonsyndromic oral clefts revisited. Cleft Palate Craniofac. J. 33, 400-417.
-
(1990)
Cleft Palate Craniofac. J.
, vol.33
, pp. 400-417
-
-
Wyszynski, D.F.1
Beaty, T.H.2
Maestri, N.3
-
44
-
-
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., Mclntosh, I., Smith, E. A., Lewanda, A. F., Garcia-Delgado, C., VinagerasGuarneros, E., Wulfsberg, E. & 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. 9, 22-20.
-
(1997)
Hum. Genet.
, vol.9
, pp. 22-120
-
-
Wyszynski, D.F.1
Maestri, N.2
Mclntosh, I.3
Smith, E.A.4
Lewanda, A.F.5
Garcia-Delgado, C.6
Vinagerasguarneros, E.7
Wulfsberg, E.8
Beaty, T.H.9
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