-
1
-
-
0030448727
-
Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly
-
Chen C-P, Liu F-F, Jan S-W, Lin C-L, Lan C-C. 1996. Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly. Clin Genet 50: 321-326.
-
(1996)
Clin Genet
, vol.50
, pp. 321-326
-
-
Chen, C.-P.1
Liu, F.-F.2
Jan, S.-W.3
Lin, C.-L.4
Lan, C.-C.5
-
2
-
-
0032831301
-
Prenatal diagnosis of partial trisomy 3p (3p23 → pter) and monosomy 7q (7q36 → qter) in a fetus with microcephaly, alobar holoprosencephaly and cyclopia
-
Chen C-P, Devriendt K, Lee C-C, Chen W-L, Wang W, Wang T-Y. 1999. Prenatal diagnosis of partial trisomy 3p (3p23 → pter) and monosomy 7q (7q36 → qter) in a fetus with microcephaly, alobar holoprosencephaly and cyclopia. Prenat Diagn 19: 986-989.
-
(1999)
Prenat Diagn
, vol.19
, pp. 986-989
-
-
Chen, C.-P.1
Devriendt, K.2
Lee, C.-C.3
Chen, W.-L.4
Wang, W.5
Wang, T.-Y.6
-
4
-
-
0023232279
-
Brief clinical report: Prenatal diagnosis of a dup(3p) with holoprosencephaly
-
Gillerot Y, Hustin J, Koulischer L, Viteux V. 1987. Brief clinical report: Prenatal diagnosis of a dup(3p) with holoprosencephaly. Am J Med Genet 26: 225-227.
-
(1987)
Am J Med Genet
, vol.26
, pp. 225-227
-
-
Gillerot, Y.1
Hustin, J.2
Koulischer, L.3
Viteux, V.4
-
5
-
-
0021965106
-
Dup(3)(p2-pter) in two families, including one infant with cyclopia
-
Gimelli G, Cuoco C, Lituania M, et al. 1985. Dup(3)(p2-pter) in two families, including one infant with cyclopia. Am J Med Genet 20: 341-348.
-
(1985)
Am J Med Genet
, vol.20
, pp. 341-348
-
-
Gimelli, G.1
Cuoco, C.2
Lituania, M.3
-
6
-
-
0026638262
-
Pallister-Hall syndrome associated with an unbalanced chromosome translocation
-
Kuller JA, Cox VA, Schonberg SA, Golabi M. 1992. Pallister-Hall syndrome associated with an unbalanced chromosome translocation. Am J Med Genet 43: 647-650.
-
(1992)
Am J Med Genet
, vol.43
, pp. 647-650
-
-
Kuller, J.A.1
Cox, V.A.2
Schonberg, S.A.3
Golabi, M.4
-
7
-
-
0027279190
-
Autosomal imbalance syndromes: Genetic interactions and the origin of congenital malformations in aneuploidy syndromes
-
Lurie IW. 1993. Autosomal imbalance syndromes: Genetic interactions and the origin of congenital malformations in aneuploidy syndromes. Am J Med Genet 47: 410-416.
-
(1993)
Am J Med Genet
, vol.47
, pp. 410-416
-
-
Lurie, I.W.1
-
8
-
-
0020626386
-
The dup(3)(p25-pter) syndrome: A case with holoprosencephaly
-
Martin JM, Steinberg BG. 1983. The dup(3)(p25-pter) syndrome: A case with holoprosencephaly. Am J Med Genet 14: 767-772.
-
(1983)
Am J Med Genet
, vol.14
, pp. 767-772
-
-
Martin, J.M.1
Steinberg, B.G.2
-
9
-
-
0034597355
-
Trisomy of 3pter in a patient with apparent C (trigonocephaly) syndrome
-
McGaughran J, Aftimos S, Oei P. 2000. Trisomy of 3pter in a patient with apparent C (trigonocephaly) syndrome. Am J Med Genet 94: 311-315.
-
(2000)
Am J Med Genet
, vol.94
, pp. 311-315
-
-
McGaughran, J.1
Aftimos, S.2
Oei, P.3
-
10
-
-
0023822528
-
Trisomy 3p23 → pter and monosomy 11q23 → qter in an infant with two translocation carrier parents
-
Neu RL, Kousseff BG, Hardy DE, et al. 1988. Trisomy 3p23 → pter and monosomy 11q23 → qter in an infant with two translocation carrier parents. J Med Genet 25: 631-633.
-
(1988)
J Med Genet
, vol.25
, pp. 631-633
-
-
Neu, R.L.1
Kousseff, B.G.2
Hardy, D.E.3
-
11
-
-
0034785353
-
Monosomy 11q: Report of new phenotypic manifestations
-
Puvabanditsin S, Garrow E, Zia-Ullah M, Supavekin S, Lianthanasarn P, Denev KI. 2001. Monosomy 11q: Report of new phenotypic manifestations. Genet Counsel 12: 283-286.
-
(2001)
Genet Counsel
, vol.12
, pp. 283-286
-
-
Puvabanditsin, S.1
Garrow, E.2
Zia-Ullah, M.3
Supavekin, S.4
Lianthanasarn, P.5
Denev, K.I.6
-
12
-
-
0003485813
-
-
Wiley-Liss: New York, NY
-
Siebert JR, Cohen MM Jr, Sulik KK, Shaw C-M, Lemire RJ. 1990. Holoprosencephaly: An Overview and Atlas of Cases. Wiley-Liss: New York, NY; 362.
-
(1990)
Holoprosencephaly: An Overview and Atlas of Cases
, pp. 362
-
-
Siebert, J.R.1
Cohen M.M., Jr.2
Sulik, K.K.3
Shaw, C.-M.4
Lemire, R.J.5
-
13
-
-
0035080163
-
Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic features
-
Smeets E, Vandenbossche L, Fryns JP. 2001. Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic features. Genet Counsel 12: 85-89.
-
(2001)
Genet Counsel
, vol.12
, pp. 85-89
-
-
Smeets, E.1
Vandenbossche, L.2
Fryns, J.P.3
-
14
-
-
0020589799
-
Partial trisomy 3p in two siblings: Clinical and pathological findings
-
Van Regemorter N, Vamos E, Gillerot Y, et al. 1983. Partial trisomy 3p in two siblings: Clinical and pathological findings. Eur J Pediatr 141: 53-56.
-
(1983)
Eur J Pediatr
, vol.141
, pp. 53-56
-
-
Van Regemorter, N.1
Vamos, E.2
Gillerot, Y.3
|