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Items: 1 to 20 of 89

1.

[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12].

Rethoré MO, Junien C, Malpuech G, Baccichetti C, Tenconi R, Kaplan JC, de Romeuf J, Lejeune J.

Ann Genet. 1976 Jun;19(2):140-2. French.

PMID:
1085604
2.

[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
3.

Identification of the origin of a 22p+ chromosome by triplex dosage effect of LDH B, GAPHD, TPI and ENO2.

Dallapiccola B, Brinchi V, Magnani M, Dacha M.

Ann Genet. 1980;23(2):111-3.

PMID:
6967283
4.
5.

12pter to 12p12.2: possible assignment of human triose phosphate isomerase.

Rethoré MO, Kaplan JC, Junien C, Lejeune J.

Hum Genet. 1977 Apr 15;36(2):235-7.

PMID:
858628
6.

Blood cell enzymes in trisomy E (18) syndrome.

Baughan MA, Sparkes RS, Paglia DE, Wilson MG.

J Med Genet. 1969 Mar;6(1):42-7. No abstract available.

7.

Human glyceraldehyde-3-phosphate dehydrogenase in man-rodent somatic cell hybrids.

Bruns GA, Gerald PS.

Science. 1976 Apr 2;192(4234):54-6.

PMID:
176725
8.

[Trisomy-21 with deficiency of erythrocyte-phosphofructokinase].

Schwarzmeier J, Moser K, Zimprich H, Weiss I.

Z Kinderheilkd. 1970;108(4):325-30. German. No abstract available.

PMID:
4252955
9.

Partial trisomy 10q in three unrelated patients.

Taysi K, Yang V, Monaghan N, Beraha N.

Ann Genet. 1983;26(2):79-85.

PMID:
6604490
10.

Resolution of breakpoints in a complex rearrangement by use of multiple staining techniques: confirmation of suspected 12p12.3 intraband by deletion dosage effect of LDHB.

Magenis E, Brown MG, Chamberlin J, Donlon T, Hepburn D, Lamvik N, Lovrien E, Yoshitomi M.

Am J Med Genet. 1981;9(2):95-103.

PMID:
6167167
11.
12.

Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases.

Kobayashi H, Montgomery KT, Bohlander SK, Adra CN, Lim BL, Kucherlapati RS, Donis-Keller H, Holt MS, Le Beau MM, Rowley JD.

Blood. 1994 Nov 15;84(10):3473-82.

13.

[Possible localization of the glutathione reductase (EC 1.6.4.2) on the 8p21 band].

Sinet PM, Bresson JL, Couturier J, Laurent C, Prieur M, Rethoré MO, Taillemite JL, Toudic D, Jérome H, Lejeune J.

Ann Genet. 1977 Mar;20(1):13-7. French.

PMID:
302667
14.

Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p.

Serville F, Junien C, Kaplan JC, Gachet M, Cadoux J, Broustet A.

Hum Genet. 1978 Nov 24;45(1):63-9.

PMID:
730182
15.

Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12.

Mayeda K, Weiss L, Lindahl R, Dully M.

Am J Hum Genet. 1974 Jan;26(1):59-64. No abstract available.

16.

[A new case of partial monosomy of chromosome 12,del(12)(p11.01 to p12.109) confirming the location of the gene for lactate dehydrogenase B].

Boilly-Dartigalongue B, Rivière D, Junien C, Couturier J, Toudic L, Marie F, Castel Y.

Ann Genet. 1985;28(1):55-7. French.

PMID:
3874590
17.

[Effect of gene dosage on the glyceraldehyde-3-phosphate dehydrogenase enzyme (GAPD) in partial 12p13.3 pter trisomy].

Barros-Núñez P, Vaca G, Sánchez-Corona J, Zúñiga G, Medina C, Rivas F, Rodríguez RM, Moller M, García-Cruz D.

Bol Med Hosp Infant Mex. 1990 Sep;47(9):656-9. Spanish.

PMID:
2271129
18.

Duplication 8p syndrome: studies in a family with a reciprocal translocation between chromosomes 8 and 12.

Moreno Fuenmayor HM, Meilinger KL, Rucknagel DL, Mohrenweiser HL, Chu EH.

Am J Med Genet. 1980;7(3):361-8.

19.

Triplex gene dosage effect of TPI and G3PD in a human lymphoblastoid cell line with partial trisomy 12p13 and 18p.

Junien C, Kaplan JC, Serville F, Lenoir G.

Hum Genet. 1979 Jun 19;49(2):221-3.

PMID:
223966
20.

Partial trisomy of the short arm of chromosome 8 resulting from balanced maternal translocation.

Jones LA, Dengler DR, Taysi K, Shackelford GD, Hartmann AF.

J Med Genet. 1980 Jun;17(3):232-5.

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