Rivera H - Search Results

1

Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy.

Rivera H, García-Esquivel L, Jiménez-Sáinz M, Vaca G, Ibarra B, Cantú JM. Rivera H, et al. Clin Genet. 1987 Jun;31(6):393-8. doi: 10.1111/j.1399-0004.1987.tb02831.x. Clin Genet. 1987. PMID: 3621643

2

De novo del(4) (p15.32) with incomplete expression of the Wolf-Hirschhorn syndrome.

Castro-Félix LP, Ramírez ML, Valera-Huezo S, Matute E, Rivas F, Rivera H, Moller M, Cantú JM. Castro-Félix LP, et al. Among authors: rivera h. Clin Genet. 1986 May;29(5):439-44. doi: 10.1111/j.1399-0004.1986.tb00518.x. Clin Genet. 1986. PMID: 2427265

3

Centric fission consequences in man.

Rivera H, Cantú JM. Rivera H, et al. Ann Genet. 1986;29(4):223-5. Ann Genet. 1986. PMID: 3495221

4

Familial trisomy 3q25----qter. Report of two cases.

Garcia-Esquivel L, Rivas F, Rivera H, Möller M, Velazquez AL, Cantu JM. Garcia-Esquivel L, et al. Among authors: rivera h. J Genet Hum. 1987 Aug;35(4):299-303. J Genet Hum. 1987. PMID: 3655754

5

Whole-arm t(X;17) (Xp17q;Xq17p) and gonadal dysgenesis. A further exception to the critical region hypothesis.

Rivera H, Enríquez-Guerra MA, Rolón A, Jiménez-Sáinz ME, Núñez-González L, Cantú JM. Rivera H, et al. Clin Genet. 1986 May;29(5):425-8. doi: 10.1111/j.1399-0004.1986.tb00515.x. Clin Genet. 1986. PMID: 3742848

6

On the origin of extra isochromosomes.

Rivera H, Rivas F, Cantú JM. Rivera H, et al. Clin Genet. 1986 Jun;29(6):540-1. doi: 10.1111/j.1399-0004.1986.tb00557.x. Clin Genet. 1986. PMID: 3742861 No abstract available.

7

Inv(4)(p16q21). A five-generation pedigree with 24 carriers and no recombinants.

Rivas F, García-Esquivel L, Rivera H, Jiménez ME, González RM, Cantú JM. Rivas F, et al. Among authors: rivera h. Clin Genet. 1987 Feb;31(2):97-101. doi: 10.1111/j.1399-0004.1987.tb02776.x. Clin Genet. 1987. PMID: 3829444

8

19q distal trisomy due to a de novo (19;22)(q13.2;p11) translocation.

Rivas F, García-Cruz D, Rivera H, Plascencia ML, González RM, Cantú JM. Rivas F, et al. Among authors: rivera h. Ann Genet. 1985;28(2):113-5. Ann Genet. 1985. PMID: 3876059

9

Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.

García-Cruz D, García-Esquivel L, Rivera H, Vaca G, Rolón A, Cantú JM. García-Cruz D, et al. Among authors: rivera h. Ann Genet. 1985;28(3):193-6. Ann Genet. 1985. PMID: 3879157

10

De novo t(4;5)(q3100;q2200) with del(5)(q1500q2200). Tentative delineation of a 5q monosomy syndrome and assignment of the critical segment.

Rivera H, Rolón A, Sánchez-Corona J, Cantú JM. Rivera H, et al. Clin Genet. 1985 Jan;27(1):105-9. doi: 10.1111/j.1399-0004.1985.tb00193.x. Clin Genet. 1985. PMID: 3978836

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