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Items: 1 to 20 of 174

1.

[Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)].

Rethoré MO, Kaplan JC, Junien C, Cruveiller J, Dutrillaux B, Aurias A, Carpentier S, Lafourcade J, Lejeune.

Ann Genet. 1975 Jun;18(2):81-7. French.

PMID:
1081369
2.
3.

The 12p trisomy syndrome.

Armendares S, Salamanca F, Nava S, Ramirez S, Cantu JM.

Ann Genet. 1975 Jun;18(2):89-94.

PMID:
1081370
4.

[Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].

Ayraud N, Galiana A, Llyod M, Deswarte M.

Ann Genet. 1976 Mar;19(1):65-8. French.

PMID:
1084126
5.

Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).

van de Vooren MJ, Planteydt HT, Hagemeijer A, Peters-Slough MF, Timmerman MJ.

Clin Genet. 1984 Jan;25(1):52-8.

PMID:
6705241
6.

A case of de novo trisomy 12p syndrome.

Ray M, Chudley AE, Christie N, Seargeant L.

Ann Genet. 1985;28(4):235-8.

PMID:
3879436
7.

[Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].

Giovannelli G, Forabosco A, Dutrillaux B.

Ann Genet. 1974 Jun;17(2):119-24. French. No abstract available.

PMID:
4547939
8.

[Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].

Turleau C, Grouchy J, Bocquentin F, Roubin M, Colin FC.

Ann Genet. 1975 Mar;18(1):41-4. French.

PMID:
1080037
9.

[Partial 7q trisomy].

Serville F, Broustet A, Sandler B, Bourdeau MJ, Leloup M.

Ann Genet. 1975 Mar;18(1):67-70. French.

PMID:
1080040
10.

Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).

Tal'vik TA, Mikel'saar AV, Mikel'saar RV.

Sov Genet. 1974 Jun 1;8(5):651-7. No abstract available.

PMID:
4413436
11.

Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).

Howard-Peebles PN, Yarbrough KM, Stoddard GR, Rary JM.

Clin Genet. 1977 Jan;11(1):46-52.

PMID:
830449
12.

Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.

Ottolina de Bracamonte N, Velazco JQ, Hammond Figueroa FG.

Acta Cient Venez. 1982;33(4):342-7. No abstract available.

PMID:
7186725
13.

Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations.

Nakai H, Yamamoto Y, Kuroki Y.

Hum Genet. 1979 Oct 2;51(3):349-55. No abstract available.

PMID:
511169
14.

Partial trisomy 9q due to maternal 9/17 translocation.

Aftimos SF, Hoo JJ, Parslow MI.

Am J Dis Child. 1980 Sep;134(9):848-50.

PMID:
7416109
15.

An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.

Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.

Hum Hered. 1973;23(6):568-85. No abstract available.

PMID:
4134631
16.

Partial trisomy 9 in the case of familial translocation 8/9 mat.

Schwanitz G, Schamberger U, Rott HD, Wieczorek V.

Ann Genet. 1974 Sep;17(3):163-6. No abstract available.

PMID:
4548816
17.

Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.

Hobolth N, Jacobsen P, Mikkelsen M.

J Med Genet. 1974 Sep;11(3):299-303. No abstract available.

18.

[Cp trisomy: a new syndrome].

Canu JM, Buentello L, Armendares S.

Ann Genet. 1971 Sep;14(3):177-86. French. No abstract available.

PMID:
5315464
19.

[Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].

Aledo AG, Gracia R, López Pajares I, González M, Oliver A, Peralta A.

An Esp Pediatr. 1982 Aug;17(2):125-9. Spanish.

PMID:
7149479
20.

12P trisomy: a syndrome?

Hoo JJ.

Ann Genet. 1976 Dec;19(4):261-3.

PMID:
1087857

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