-
1
-
-
0025941775
-
De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: Clinical significance and distribution of breakpoints
-
Warburton D. De novo balanced chromosome rearrangements and extra marker chromosomes identifed at prenatal diagnosis: clinical signifcance and distribution of breakpoints. Am J Med Genet 49:995-1013, 1991. (Pubitemid 21891747)
-
(1991)
American Journal of Human Genetics
, vol.49
, Issue.5
, pp. 995-1013
-
-
Warburton, D.1
-
2
-
-
66849099873
-
Etiology of nonimmune hydrops fetalis: A systematic review
-
Bellini C, Hennekam RCM, Fulcheri E, Rutigliani M, Morcaldi G, Boccardo F, Bonioli E. 2009. Etiology of nonimmune hydrops fetalis: A systematic review. Am J Med Genet Part A 149A:844-851.
-
(2009)
Am J Med Genet Part A
, vol.149 A
, pp. 844-851
-
-
Bellini, C.1
Hennekam, R.C.M.2
Fulcheri, E.3
Rutigliani, M.4
Morcaldi, G.5
Boccardo, F.6
Bonioli, E.7
-
3
-
-
0024347013
-
Hydrops revisited: Literature review of 1, 414 cases published in the 1980s
-
Machin GA. Hydrops revisited: literature review of 1, 414 cases published in the 1980s. Am J Med Genet 34:366-390, 1989.
-
(1989)
Am J Med Genet
, vol.34
, pp. 366-390
-
-
MacHin, G.A.1
-
4
-
-
66149110775
-
Case 16-2009: A 32-year-old pregnant woman with an abnormal fetal ultrasound study
-
Lockwood CJ, Nadel AS, King MA, Roberts DJ. Case 16-2009: a 32-year-old pregnant woman with an abnormal fetal ultrasound study. N Engl J Med 360:2225-2235, 2009.
-
(2009)
N Engl J Med
, vol.360
, pp. 2225-2235
-
-
Lockwood, C.J.1
Nadel, A.S.2
King, M.A.3
Roberts, D.J.4
-
5
-
-
0025108240
-
Premature centromere division of a translocation-carrier autosome
-
Mehes K, Kosztolanyi G. Premature centromere division of a translocation-carrier autosome. Hum Genet 85:379-380, 1990. (Pubitemid 20279568)
-
(1990)
Human Genetics
, vol.85
, Issue.3
, pp. 379-380
-
-
Mehes, K.1
Kosztolanyi, G.2
-
6
-
-
0025964924
-
A familial MCA/MR syndrome due to translocation t(10;16)(q26;p13. 1): Report of six cases
-
Bofnger MK, Opitz JM, Soukup SW, Ekblom LS, Phillips S, Daniel A, Greene EW. A familial MCA/MR syndrome due to translocation t(10;16)(q26;p13. 1): report of six cases. Am J Med Genet 38:1-8, 1991.
-
(1991)
Am J Med Genet
, vol.38
, pp. 1-8
-
-
Bofnger, M.K.1
Opitz, J.M.2
Soukup, S.W.3
Ekblom, L.S.4
Phillips, S.5
Daniel, A.6
Greene, E.W.7
-
8
-
-
18744432675
-
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features
-
DOI 10.1002/1097-0223(20000 6)20:6<511::AID-PD84 9>3.0.CO;2-B
-
Fert-Ferrer S, Guichet A, Tantau J, Delezoide AL, Ozilou C, Romana SP, Gosset P, Viot G, Loison S, Moraine C, Morichon-Delvallez N, Turleau C, Vekemans M, Prieur M. Subtle familial unbalanced translocation t(8;11)(p23. 2;p15. 5) in two fetuses with Beckwith-Wiedemann features. Prenat Diagn 20:511-515, 2000. (Pubitemid 30394280)
-
(2000)
Prenatal Diagnosis
, vol.20
, Issue.6
, pp. 511-515
-
-
Fert-Ferrer, S.1
Guichet, A.2
Tantau, J.3
Delezoide, A.L.4
Ozilou, C.5
Romana, S.P.6
Gosset, P.7
Viot, G.8
Loison, S.9
Moraine, C.10
Morichon-Delvallez, N.11
Turleau, C.12
Vekemans, M.13
Prieur, M.14
-
9
-
-
0029874214
-
Nonimmune fetal hydrops and placentomegaly: Diagnosis of familial wiedemann-beckwith syndrome with trisomy 11p15 using fish
-
Drut RM, Drut R. Nonimmune fetal hydrops and placentomegaly: diagnosis of familial Wiedemann-Beckwith syndrome with trisomy 11p15 using FISH. Am J Med Genet 62:145-149, 1996.
-
(1996)
Am J Med Genet
, vol.62
, pp. 145-149
-
-
Drut, R.M.1
Drut, R.2
-
10
-
-
0022899565
-
18q+, the progeny of a balanced translocation t(1;18)mat: Case report with necropsy findings
-
Hindi A, Beneck D, Greco MA, Wolman SR. 18q+, theprogeny ofabalanced translocation t(1;18)mat: case report with necropsy fndings. Journal of Medical Genetics 23(3):263-266, 1986. (Pubitemid 16077091)
-
(1986)
Journal of Medical Genetics
, vol.23
, Issue.3
, pp. 263-266
-
-
Hindi, A.1
Beneck, D.2
Greco, M.A.3
Wolman, S.R.4
-
11
-
-
0018289839
-
Partial duplication of the long arm of chromosome 5: A case due to balanced paternal translocation and review of the literature
-
DOI 10.1007/BF00278289
-
Jones LA, Jordan DK, Taysi K, Strauss AW, Toth JK. Partial duplication of the long arm of chromosome 5: a case due to balanced paternal translocation and review of the literature. Hum Genet 51:37-42, 1979. (Pubitemid 9242108)
-
(1979)
Human Genetics
, vol.51
, Issue.1
, pp. 37-42
-
-
Jones, L.A.1
Jordan, D.K.2
Taysi, K.3
-
12
-
-
0018867191
-
A clinical syndrome associated with 5p duplication and 9p deletion
-
Liberfarb RM, Atkins L, Holmes LB. A clinical syndrome associated with 5p duplication and 9p deletion. Annales de Genetique 23:26-30, 1980. (Pubitemid 10117624)
-
(1980)
Annales de Genetique
, vol.23
, Issue.1
, pp. 26-30
-
-
Liberfarb, R.M.1
Atkins, L.2
Holmes, L.B.3
-
13
-
-
0021070666
-
Mating between two balanced translocation carriers in two unrelated families
-
Dallapiccola B, Chessa L, Brinchi V, Frontali M, Gandini E. Mating between two balanced transloca-tion carriers in two unrelated families. Hum Genet 65:165-168, 1983. (Pubitemid 14210637)
-
(1983)
Human Genetics
, vol.65
, Issue.2
, pp. 165-168
-
-
Dallapiccola, B.1
Chessa, L.2
Brinchi, V.3
|