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Items: 1 to 50 of 59

1.

Balanced complex chromosome rearrangement ascertained through prenatal diagnosis.

Farrell SA, Summers AM, Gardner HA, Uchida IA.

Am J Med Genet. 1994 Sep 1;52(3):360-1. No abstract available.

PMID:
7810570
2.

Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents.

Uchida IA, Freeman VC.

Hum Genet. 1986 Feb;72(2):118-22.

PMID:
2935479
3.

The fragile X in cattle.

Uchida IA, Freeman VC, Basrur PK.

Am J Med Genet. 1986 Jan-Feb;23(1-2):557-62.

PMID:
3456707
4.

Detection and interpretation of two different cell lines in triploid abortions.

Uchida IA, Freeman VC, Chen PL.

Clin Genet. 1985 Dec;28(6):489-94.

PMID:
4075560
5.

Triploidy and chromosomes.

Uchida IA, Freeman VC.

Am J Obstet Gynecol. 1985 Jan 1;151(1):65-9.

PMID:
3966508
6.

Trisomy 21 Down syndrome. Parental mosaicism.

Uchida IA, Freeman VC.

Hum Genet. 1985;70(3):246-8.

PMID:
3160645
7.

Twinning rate in spontaneous abortions.

Uchida IA, Freeman VC, Gedeon M, Goldmaker J.

Am J Hum Genet. 1983 Sep;35(5):987-93.

8.

Additional evidence for fragile X activity in heterozygous carriers.

Uchida IA, Freeman VC, Jamro H, Partington MW, Soltan HC.

Am J Hum Genet. 1983 Sep;35(5):861-8.

9.

Birth weight and placental proximity in like-sexed twins.

Buzzard IM, Uchida IA, Norton JA Jr, Christian JC.

Am J Hum Genet. 1983 Mar;35(2):318-23.

10.

45,X/46,XX mosaicism in discordant monozygotic twins.

Uchida IA, deSa DJ, Whelan DT.

Pediatrics. 1983 Mar;71(3):413-7.

PMID:
6572357
11.

Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33.

Tomkins DJ, Hunter AG, Uchida IA, Roberts MH.

Clin Genet. 1982 Dec;22(6):348-55.

PMID:
7160106
12.

Activity of the fragile X in heterozygous carriers.

Uchida IA, Joyce EM.

Am J Hum Genet. 1982 Mar;34(2):286-93.

13.

Partial 11q trisomy syndrome.

Pihko H, Therman E, Uchida IA.

Hum Genet. 1981;58(2):129-34.

PMID:
7286998
14.

Placentation effects on cognitive resemblance of adult monozygotes.

Rose RJ, Uchida IA, Christian JC.

Prog Clin Biol Res. 1981;69 Pt B:35-41. No abstract available.

PMID:
7199174
15.

A rare case of mosaic Down syndrome 46,XY/46,XY, -21, +i(21q).

Uchida IA, Whelan DT.

Clin Genet. 1980 Apr;17(4):271-4.

PMID:
6445245
16.

Radiation-induced nondisjunction.

Uchida IA.

Environ Health Perspect. 1979 Aug;31:13-17.

17.

Comparisons of dermatoglyphic patterns in monochorionic and dichorionic monozygotic twins.

Reed T, Uchida IA, Norton JA Jr, Christian JC.

Am J Hum Genet. 1978 Jul;30(4):383-91.

18.

Radiation-induced nondisjunction in oocytes of aged mice.

Uchida IA, Freeman CP.

Nature. 1977 Jan 13;265(5590):186-7. No abstract available.

PMID:
834262
19.

Letter: Confirmation of trisomy 22 with fluorescence banding.

Uchida IA, Byrnes EM.

Am J Hum Genet. 1976 Mar;28(2):189-90. No abstract available.

20.

Centromeric linkage in trisomy 21.

Côté GB, Edwards JH, Chown B, Giblett ER, Lewis M, Moore BP, Steinberg AG, Uchida IA.

Ann Hum Genet. 1975 Jul;39(1):61-6. No abstract available.

PMID:
1180487
21.
22.

Radiation-induced chromosome aberrations in mouse spermatocytes and oocytes.

Tsuchida RS, Uchida IA.

Cytogenet Cell Genet. 1975;14(1):1-8.

PMID:
1132245
23.

Letter: Rapid chromosome diagnosis.

Lee CP, Macmillan AB, Uchida IA, Yeung CY.

Lancet. 1974 Sep 21;2(7882):716. No abstract available.

PMID:
4142982
24.

Radiation-induced nondisjunction in mouse oocytes.

Uchida IA, Lee CP.

Nature. 1974 Aug 16;250(467):601-2. No abstract available.

PMID:
4845661
25.
26.

Chromosome aberrations in spermatocytes and oocytes of mice irradiated prenatally.

Tsuchida WS, Uchida IA.

Mutat Res. 1974 Mar;22(3):277-80. No abstract available.

PMID:
4536416
27.

Identification of partial 12 trisomy by quinacrine fluorescence.

Uchida IA, Lin CC.

J Pediatr. 1973 Feb;82(2):269-72. No abstract available.

PMID:
4119313
28.

Identification of triploid genome by fluorescence microscopy.

Uchida IA, Lin CC.

Science. 1972 Apr 21;176(4032):304-5.

PMID:
5019785
29.

Ring formation of chromosomes nos. 19 and 20.

Uchida IA, Lin CC.

Cytogenetics. 1972;11(3):208-15. No abstract available.

PMID:
5038363
30.
31.

A suggestion for the nomenclature of the fluorescent banding patterns in human metaphase chromosomes.

Lin CC, Uchida IA, Byrnes E.

Can J Genet Cytol. 1971 Jun;13(2):361-3. No abstract available.

PMID:
5125646
32.

Trisomy associated with diagnostic X-rays.

Uchida IA.

South Med J. 1971 Feb;64:Suppl1:81-4. No abstract available.

PMID:
5542309
33.

Immunological profile in a chromosome 18 deletion syndrome with IgA deficiency.

Finley SC, Cooper MD, Finley WH, Uchida IA, Noto TA, Roddam RF.

J Med Genet. 1969 Dec;6(4):388-93. No abstract available.

34.

Sex-linked congenital deafness.

McRae KN, Uchida IA, Lewis M.

Am J Hum Genet. 1969 Sep;21(5):415-22. No abstract available.

35.

Selection for trisomic cells in a mosaic fibroblast culture.

Chang TD, Niewczas-Late V, Uchida IA.

Cytogenetics. 1969;8(6):410-4. No abstract available.

PMID:
5365246
36.

Maternal radiation and chromosomal aberrations.

Uchida IA, Holunga R, Lawler C.

Lancet. 1968 Nov 16;2(7577):1045-9. No abstract available.

PMID:
4176862
37.

IgA absence associated with a ring-18 chromosome.

Finley SC, Finley WH, Noto TA, Uchida IA, Roddam RF.

Lancet. 1968 May 18;1(7551):1095-6. No abstract available.

PMID:
4171782
38.

Familial occurrence of trisomy 22.

Uchida IA, Ray M, McRae KN, Besant DF.

Am J Hum Genet. 1968 Mar;20(2):107-18. No abstract available.

39.

Dermatoglyphics and chromosomes.

Uchida IA.

Ala J Med Sci. 1966 Oct;3(4):432-4. No abstract available.

PMID:
5978174
40.

21 trisomy with an XYY sex chromosome complement.

Uchida IA, Ray M, Ducan BP.

J Pediatr. 1966 Aug;69(2):295-8. No abstract available.

PMID:
5946659
41.

Mail-order chromosome analysis.

Uchida IA, Ray M.

Can Med Assoc J. 1966 Mar 26;94(13):649-50.

42.

Increased frequency of thyroid autoantibodies in mothers of patients with Down's syndrome.

Fialkow PJ, Hecht F, Uchida IA, Motulsky AG.

Lancet. 1965 Oct 30;2(7418):868-70. No abstract available.

PMID:
4158240
43.

FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

UCHIDA IA, MCRAE KN, RAY M.

Am J Hum Genet. 1965 Sep;17:410-9. No abstract available.

44.

The diagnostic value of dermatoglyphics in a defective delinquent with two extra chromosomes.

Bray PF, Ann Josephine Sister, Uchida IA.

Trans Am Neurol Assoc. 1965;90:234. No abstract available.

PMID:
5857749
45.

DIZYGOTIC TWINS WITH XX-XY CHIMERISM.

UCHIDA IA, WANG HC, RAY M.

Nature. 1964 Oct 10;204:191. No abstract available.

PMID:
14222273
46.

DERMATOGLYPHICS ASSOCIATED WITH THE XXYH CHROMOSOME COMPLEMENT.

UCHIDA IA, MILLER JR, SOLTAN HC.

Am J Hum Genet. 1964 Sep;16:284-91. No abstract available.

47.

PARTIAL TRISOMY-DEFICIENCY SYNDROME RESULTING FROM A RECIPROCAL TRANSLOCATION IN A LARGE KINDRED.

UCHIDA IA, WANG HC, LAXDAL OE, ZALESKI WA, DUNCAN BP.

Cytogenetics. 1964;3:81-96. No abstract available.

PMID:
14190616
48.

A review of the 18 trisomy syndrome.

GIBSON DA, UCHIDA IA, LEWIS AJ.

Med Biol Illus. 1963 Apr;13:80-8. No abstract available.

PMID:
13947714
49.

The effect of maternal age and radiation on the rate of non-disjunction in Drosophila melanogaster.

UCHIDA IA.

Can J Genet Cytol. 1962 Dec;4:402-8. No abstract available.

PMID:
13995081
50.

Dermal patterns of 18 and D1 trisomics.

UCHIDA IA, PATAU K, SMITH DW.

Am J Hum Genet. 1962 Dec;14:345-52. No abstract available.

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