-
1
-
-
0026683264
-
Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndrome
-
Bonaventure J, Lasselin C, Mellier J, Cohen-Solal L, Maroteaux P: Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndrome. J Med Genet 1992;29:465-470.
-
(1992)
J Med Genet
, vol.29
, pp. 465-470
-
-
Bonaventure, J.1
Lasselin, C.2
Mellier, J.3
Cohen-Solal, L.4
Maroteaux, P.5
-
2
-
-
0000169436
-
Multiple congenital dislocations associated with characteristic facial abnormality
-
Larsen LJ, Schottstaedt ER, Bost FC: Multiple congenital dislocations associated with characteristic facial abnormality. J Pediatr 1950;37:574-581.
-
(1950)
J Pediatr
, vol.37
, pp. 574-581
-
-
Larsen, L.J.1
Schottstaedt, E.R.2
Bost, F.C.3
-
3
-
-
0015315531
-
Larsen syndrome: Congenital dislocation of the knees and other joints, distinctive facies, and frequently cleft palate
-
Silverman FN: Larsen syndrome: Congenital dislocation of the knees and other joints, distinctive facies, and frequently cleft palate. Ann Radiol 1972;15:297-328.
-
(1972)
Ann Radiol
, vol.15
, pp. 297-328
-
-
Silverman, F.N.1
-
4
-
-
0025758451
-
Prenatal diagnosis of recurrent Larsen syndrome: Further definition of a lethal variant
-
Mostello D, Hoechstetter L, Bendon RW, Dignan PStJ, Oestreich AE, Siddiqi TA: Prenatal diagnosis of recurrent Larsen syndrome: Further definition of a lethal variant. Prenat Diagn 1991;11:215-225.
-
(1991)
Prenat Diagn
, vol.11
, pp. 215-225
-
-
Mostello, D.1
Hoechstetter, L.2
Bendon, R.W.3
Pstj, D.4
Oestreich, A.E.5
Siddiqi, T.A.6
-
5
-
-
0025946356
-
Two unrelated children with partial trisomy Iq and monosomy 6p, presenting with the phenotype of the Larsen syndrome
-
Pierquin G, van Regemorter N, Hayes Dealte G, Fourneau C, Foerster M, Damis E, Cremer-Perlmutter V: Two unrelated children with partial trisomy Iq and monosomy 6p, presenting with the phenotype of the Larsen syndrome. Hum Genet 1991;87:587-591.
-
(1991)
Hum Genet
, vol.87
, pp. 587-591
-
-
Pierquin, G.1
Van Regemorter, N.2
Hayes Dealte, G.3
Fourneau, C.4
Foerster, M.5
Damis, E.6
Cremer-Perlmutter, V.7
-
8
-
-
0027530357
-
Larsen syndrome presenting as a familial syndrome of dwarfism, distinct oldish facial appearance and bilateral clubfeet in mother and daughter
-
Fryns JP, Lenaerts J, van den Berghe H: Larsen syndrome presenting as a familial syndrome of dwarfism, distinct oldish facial appearance and bilateral clubfeet in mother and daughter. Genet Couns 1993;4:43-46.
-
(1993)
Genet Couns
, vol.4
, pp. 43-46
-
-
Fryns, J.P.1
Lenaerts, J.2
Van Den Berghe, H.3
-
9
-
-
0027228360
-
Long-term follow-up of two sibs with Larsen syndrome possibly due to parental germ-mosaicism
-
Petrella R, Rabinowitz JG, Steinmann B, Hirschhorn K: Long-term follow-up of two sibs with Larsen syndrome possibly due to parental germ-mosaicism. Am J Med Genet 1993;47:187-197.
-
(1993)
Am J Med Genet
, vol.47
, pp. 187-197
-
-
Petrella, R.1
Rabinowitz, J.G.2
Steinmann, B.3
Hirschhorn, K.4
-
10
-
-
0027270019
-
Prenatal diagnosis and obstetric management of Larsen syndrome
-
Rochelson B, Petrikovsky B, Shmoys S: Prenatal diagnosis and obstetric management of Larsen syndrome. Obstet Gynecol 1993;81:845-847.
-
(1993)
Obstet Gynecol
, vol.81
, pp. 845-847
-
-
Rochelson, B.1
Petrikovsky, B.2
Shmoys, S.3
-
11
-
-
0028275607
-
A case of Larsen syndrome with severe cervical malformations
-
Le Marec B, Chapuis M, Treguier C, Odent S, Bracq H: A case of Larsen syndrome with severe cervical malformations. Genet Couns 1994;5:179-181.
-
(1994)
Genet Couns
, vol.5
, pp. 179-181
-
-
Le Marec, B.1
Chapuis, M.2
Treguier, C.3
Odent, S.4
Bracq, H.5
-
13
-
-
0027991760
-
A case of Larsen syndrome with severe cervical cord compression
-
Sumitani S, Kameda K, Sone S, Minami R: A case of Larsen syndrome with severe cervical cord compression. No To Hattatsu 1994;26:345-348.
-
(1994)
No to Hattatsu
, vol.26
, pp. 345-348
-
-
Sumitani, S.1
Kameda, K.2
Sone, S.3
Minami, R.4
-
15
-
-
0028865040
-
Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus
-
Vujic M, Hallstensson K., Wahlström J, Lund-Berg A, Langmaack C, Martinsson T: Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus. Am J Hum Genet 1995;57:1104-1113.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1104-1113
-
-
Vujic, M.1
Hallstensson, K.2
Wahlström, J.3
Lund-Berg, A.4
Langmaack, C.5
Martinsson, T.6
-
17
-
-
0030000414
-
Anesthetic implications of Larsen syndrome
-
Tobias JD: Anesthetic implications of Larsen syndrome. J Clin Anesth 1996;8:255-257.
-
(1996)
J Clin Anesth
, vol.8
, pp. 255-257
-
-
Tobias, J.D.1
-
18
-
-
0003436550
-
-
Baltimore, Johns Hopkins University Press
-
McKusick VA: Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and x-Linked Phenotypes, ed 10. Baltimore, Johns Hopkins University Press, 1992, pp 651-652, 1497.
-
(1992)
Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes, Ed 10
, pp. 651-652
-
-
McKusick, V.A.1
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