-
1
-
-
0030035153
-
Genomic structure of HOXD13 gene: A nine polyalanine duplication causes synpolydactyly in two unrelated families
-
Akarsu AN, Stoiov I, Yilmaz E, Sayli BS, Sarfarazi M (1996). Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families. Hum Molec Genet 5:945-952.
-
(1996)
Hum Molec Genet
, vol.5
, pp. 945-952
-
-
Akarsu, A.N.1
Stoiov, I.2
Yilmaz, E.3
Sayli, B.S.4
Sarfarazi, M.5
-
2
-
-
0035093474
-
Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLIN
-
Bacchelli C, Goodman FR, Scambler PJ, Winter RM (2001). Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLIN. Clin Genet 59:203-205.
-
(2001)
Clin Genet
, vol.59
, pp. 203-205
-
-
Bacchelli, C.1
Goodman, F.R.2
Scambler, P.J.3
Winter, R.M.4
-
4
-
-
0014186092
-
Total syndaktylie und totale radioulnare synostose bie zwei bruedern. Ein beitrog zur genetik der syndaktylien
-
Cenani A, Lenz W (1967). Total Syndaktylie und totale radioulnare synostose bie zwei Bruedern. Ein Beitrog zur Genetik der Syndaktylien. Ztschr Kinderheilk 101:181-190.
-
(1967)
Ztschr Kinderheilk
, vol.101
, pp. 181-190
-
-
Cenani, A.1
Lenz, W.2
-
5
-
-
0031666281
-
Physical mapping of the t(12;22)translocation break points in a family with a complex type of 3/3 phine/4 synpolydactyly
-
Debeer P, Schoenmakers EFPM, Thoelen R, Fryns J-P, Van der Ven WJM (1998). Physical mapping of the t(12;22)translocation break points in a family with a complex type of 3/3 phine/4 synpolydactyly. Cytogenet Cell Genet 81:229-234.
-
(1998)
Cytogenet Cell Genet
, vol.81
, pp. 229-234
-
-
Debeer, P.1
Schoenmakers, E.F.P.M.2
Thoelen, R.3
Fryns, J.-P.4
Van Der Ven, W.J.M.5
-
6
-
-
0033902058
-
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint
-
Debeer P, Schoenmakers EF, Thoelen R, Holvoet M (2000). Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint. Eur J Hum Genet 8:561-570.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 561-570
-
-
Debeer, P.1
Schoenmakers, E.F.2
Thoelen, R.3
Holvoet, M.4
-
7
-
-
0036171086
-
The Fibulin-1 gene (FBLN1) is disrupted in a t(12,22) associated with a complex type of synpolydactyly
-
Debeer P, Schoenmakers EF, Twal WO, Argraves WS, De Smet L, Fryns JP, Van De Ven WJ (2002). The Fibulin-1 gene (FBLN1) is disrupted in a t(12,22) associated with a complex type of synpolydactyly. J Med Genet 39:98-104.
-
(2002)
J Med Genet
, vol.39
, pp. 98-104
-
-
Debeer, P.1
Schoenmakers, E.F.2
Twal, W.O.3
Argraves, W.S.4
De Smet, L.5
Fryns, J.P.6
Van De Ven, W.J.7
-
8
-
-
0026660287
-
Cenani-Lenz type of syndactyly: A complex type of syndactyly with multiple synostoses
-
DeSemet B, Winnepenninckx B, Fryns JP, Fabry G (1992). Cenani-Lenz type of syndactyly: a complex type of syndactyly with multiple synostoses. Genet Counsel 3:145-147.
-
(1992)
Genet Counsel
, vol.3
, pp. 145-147
-
-
DeSemet, B.1
Winnepenninckx, B.2
Fryns, J.P.3
Fabry, G.4
-
9
-
-
0029901276
-
Cenani-Lenz syndrome in father and daughter
-
DeSemet L, Debeer P, Fryns JP (1996). Cenani-Lenz syndrome in father and daughter. Genet Counsel 7:153-157.
-
(1996)
Genet Counsel
, vol.7
, pp. 153-157
-
-
DeSemet, L.1
Debeer, P.2
Fryns, J.P.3
-
10
-
-
0018644417
-
Oligodactyly and multiple synostoses of the extremities: Two cases in sibs. A variant of Cenani-Lenz syndactyly
-
Dodinval P (1979). Oligodactyly and multiple synostoses of the extremities: two cases in sibs. A variant of Cenani-Lenz syndactyly. Hum Genet 48:183-189.
-
(1979)
Hum Genet
, vol.48
, pp. 183-189
-
-
Dodinval, P.1
-
11
-
-
0017214445
-
Totale syndaktylie mit mesomeler armverkerzung, radioulnaeren und metacarpalen synostosen und disorganisation der phalengen (Cenani-Syndaktylie)
-
Drohm D, Lenz W, Yang TS (1976). Totale Syndaktylie mit mesomeler Armverkerzung, radioulnaeren und metacarpalen Synostosen und Disorganisation der Phalengen (Cenani-Syndaktylie). Klin Paediat 188:359-365.
-
(1976)
Klin Paediat
, vol.188
, pp. 359-365
-
-
Drohm, D.1
Lenz, W.2
Yang, T.S.3
-
12
-
-
0030986584
-
Dermatoglyphics in patients with Cenani-Lenz type syndactyly: Studies in a new case
-
Elcioglu N, Atasu M, Cenani A (1997). Dermatoglyphics in patients with Cenani-Lenz type syndactyly: studies in a new case. Am J Med Genet 70:341-345.
-
(1997)
Am J Med Genet
, vol.70
, pp. 341-345
-
-
Elcioglu, N.1
Atasu, M.2
Cenani, A.3
-
13
-
-
0038374081
-
-
Personal communication to Temtamy and Mckuscik (1978)
-
Lenz W (1973). Personal communication to Temtamy and Mckuscik (1978).
-
(1973)
-
-
Lenz, W.1
-
14
-
-
0038712399
-
Uber glichzcitiges vorkommen von gliedmassende- fikten und osteosklerotischer systemerkrankung
-
Liebenam L (1983). Uber glichzcitiges Vorkommen von Gliedmassende- fikten und osteosklerotischer Systemerkrankung. Z Mensch Vererbungs Konstitionslehre 21:697-703.
-
(1983)
Z Mensch Vererbungs Konstitionslehre
, vol.21
, pp. 697-703
-
-
Liebenam, L.1
-
15
-
-
0036018134
-
Cenani-Lenz syndrome: Report of a new case and review of the literature
-
Nezarati MM, Mcleod DR (2002). Cenani-Lenz syndrome: report of a new case and review of the literature. Clin Dysmorphol 11:215-218.
-
(2002)
Clin Dysmorphol
, vol.11
, pp. 215-218
-
-
Nezarati, M.M.1
Mcleod, D.R.2
-
16
-
-
0040920369
-
-
OMIM (T.M) Center for Medical Genetics, John Hopkins University (Baltimore, M.D) and the National Library of Medicine (Bethesda, M.D)
-
OMIM online Mendalian Inheritance in Man. OMIM (T.M) Center for Medical Genetics, John Hopkins University (Baltimore, M.D) and the National Library of Medicine (Bethesda, M.D) www.ncbi.nlm.nih.gov/omim.
-
OMIM Online Mendalian Inheritance in Man
-
-
-
17
-
-
0020078323
-
Present nosology of the Cenani-Lenz type of syndactyly
-
Pfeiffer RA, Meisel-Stosiek M (1982). Present nosology of the Cenani-Lenz type of syndactyly. Clin Genet 21:74-79.
-
(1982)
Clin Genet
, vol.21
, pp. 74-79
-
-
Pfeiffer, R.A.1
Meisel-Stosiek, M.2
-
18
-
-
0026950938
-
Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy
-
Richard I, Broux O, Hillaire D, et al. (1992). Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy. Hum Mol Genet 1:621-624.
-
(1992)
Hum Mol Genet
, vol.1
, pp. 621-624
-
-
Richard, I.1
Broux, O.2
Hillaire, D.3
-
19
-
-
0343775662
-
A variant of Cenani-Lenz type syndactyly
-
Seven M, Yuksel A, Ozkilic A, et al. (2000). A variant of Cenani-Lenz type syndactyly. Genet Counsel 11:41-47.
-
(2000)
Genet Counsel
, vol.11
, pp. 41-47
-
-
Seven, M.1
Yuksel, A.2
Ozkilic, A.3
-
20
-
-
0013656160
-
The genetics of hand malformations
-
The National Foundation- March of Dimes, New York, Alan R. Liss Inc
-
Temtamy S, McKusick V (1978). The Genetics of Hand Malformations. Birth Defects Original Article Series XIV(3). The National Foundation- March of Dimes, New York, Alan R. Liss Inc, pp. 320-322.
-
(1978)
Birth Defects Original Article Series
, vol.14
, Issue.3
, pp. 320-322
-
-
Temtamy, S.1
McKusick, V.2
-
21
-
-
0017285716
-
Split hand and split foot deformity inherited as autosomal recessive trait
-
Verma IC, Joseph R, Bhargava S, Mehta S (1976). Split hand and split foot deformity inherited as autosomal recessive trait. Clin Genet 9:8-14.
-
(1976)
Clin Genet
, vol.9
, pp. 8-14
-
-
Verma, I.C.1
Joseph, R.2
Bhargava, S.3
Mehta, S.4
-
22
-
-
0023720768
-
Malformation syndrome: A review of mouse/human homology
-
Winter RM (1988). Malformation syndrome: a review of mouse/human homology. J Med Genet 25:480-487.
-
(1988)
J Med Genet
, vol.25
, pp. 480-487
-
-
Winter, R.M.1
-
23
-
-
0001790403
-
Certain congenital limb defficiencies occurring in twins and half-sibling
-
Yelton CI (1962). Certain congenital limb defficiencies occurring in twins and half-sibling. Inter-Clinic Inform Bull 1:1-7.
-
(1962)
Inter-Clinic Inform Bull
, vol.1
, pp. 1-7
-
-
Yelton, C.I.1
|