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Items: 1 to 20 of 21

1.

Chromosomal aberrations in couples undergoing intracytoplasmic sperm injection: influence on implantation and ongoing pregnancy rates.

Scholtes MC, Behrend C, Dietzel-Dahmen J, van Hoogstraten DG, Marx K, Wohlers S, Verhoeven H, Zeilmaker GH.

Fertil Steril. 1998 Nov;70(5):933-7.

PMID:
9806579
2.

Parental chromosome translocations and fetal loss.

Tsenghi C, Metaxotou C, Kalpini-Mavrou A, Strataki-Benetou M, Matsaniotis N.

Obstet Gynecol. 1981 Oct;58(4):456-8.

PMID:
7279340
3.

Duplication deficiency as the result of meiotic segregation of a maternal InV (10).

Yunis E, Torres de Caballero O.

Hum Genet. 1981;57(1):71-4.

PMID:
7262871
4.

Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26).

Lansky-Shafer SC, Daniel WL, Ruiz L.

J Med Genet. 1981 Feb;18(1):59-61.

5.

Regional mapping of the locus for hexokinase-1 (HK1) to 10p11 equals to q23 by gene dosage in human fibroblasts.

Gitelman BJ, Simpson NE.

Hum Genet. 1982;60(3):227-9. No abstract available.

PMID:
7106753
6.

Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).

Gonzalez CH, Billerbeck AE, Takayama LC, Wajntal A.

Am J Med Genet. 1983 Jan;14(1):159-67.

PMID:
6829605
7.

[Familial pericentric inversion of chromosome 10. 2 new cases].

Teyssier M, Moreau N.

Ann Genet. 1983;26(3):183-6. French.

PMID:
6606382
8.
9.

Clinicopathological conference: a newborn monozygotic twin with abnormal facial appearance and respiratory insufficiency.

Juberg RC, Stallard R, Straughen WJ, Avotri KJ, Washington JW.

Am J Med Genet. 1981;10(2):193-200.

PMID:
6119027
10.

Pericentric inversions of human chromosomes 9 and 10.

de la Chapelle A, Schröder J, Stenstrand K, Fellman J, Herva R, Saarni M, Anttolainen I, Tallila I, Tervilä L, Husa L, Tallqvist G, Robson EB, Cook PJ, Sanger R.

Am J Hum Genet. 1974 Nov;26(6):746-66. No abstract available.

11.

Prenatal diagnosis of trisomy 10 p in a twin pregnancy.

Farge P, Dallaire L, Potier M, Melançon SB.

Prenat Diagn. 1985 May-Jun;5(3):199-203.

PMID:
4022943
12.

Pericentric inversions in man: personal experience and review of the literature.

Kleczkowska A, Fryns JP, Van den Berghe H.

Hum Genet. 1987 Apr;75(4):333-8.

PMID:
3570287
14.

Translocations are infrequent among couples having repeated spontaneous abortions but no other abnormal pregnancies.

Simpson JL, Meyers CM, Martin AO, Elias S, Ober C.

Fertil Steril. 1989 May;51(5):811-4.

PMID:
2707455
15.

Early amniocentesis: report of 407 cases with neonatal follow-up.

Penso CA, Sandstrom MM, Garber MF, Ladoulis M, Stryker JM, Benacerraf BB.

Obstet Gynecol. 1990 Dec;76(6):1032-6.

PMID:
2234711
17.

Partial deletion 10p syndrome. Report of two patients.

Obregon MG, Mingarelli R, Giannotti A, di Comite A, Spedicato FS, Dallapiccola B.

Ann Genet. 1992;35(2):101-4.

PMID:
1524405
18.

Trisomy of the short arm of chromosome 10.

Nakagome Y, Kobayashi H.

J Med Genet. 1975 Dec;12(4):412-4.

19.

Trisomy iop.

Yunis E, Silva R, Giraldo A.

Ann Genet. 1976 Mar;19(1):57-60.

PMID:
1084124
20.

Brother and sister with trisomy 10p. 46,XY,(22p+)mat; 46,XX,(22p+)mat.

de Chieri P, Spatuzza E, Bonich JM.

Hum Genet. 1978 Nov 24;45(1):71-5.

PMID:
730183
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