Tharapel AT[au] - Search Results

Year	Number of Results
1977	3
1978	1
1983	1
1984	1
1985	1
1986	5
1989	4
1990	6
1991	5
1992	3
1993	6
1994	1
1995	1
1996	3
1997	5
1998	4
1999	2
2000	5
2002	3
2006	3
2024	0

1

Recurrent pregnancy losses and parental chromosome abnormalities: a review.

Tharapel AT, Tharapel SA, Bannerman RM. Tharapel AT, et al. Br J Obstet Gynaecol. 1985 Sep;92(9):899-914. doi: 10.1111/j.1471-0528.1985.tb03069.x. Br J Obstet Gynaecol. 1985. PMID: 3899162 Review.

2

Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.

Pivnick EK, Wilroy RS, Summitt JB, Tucker B, Herrod HG, Tharapel AT. Pivnick EK, et al. Among authors: tharapel at. Am J Med Genet. 1990 Sep;37(1):92-6. doi: 10.1002/ajmg.1320370121. Am J Med Genet. 1990. PMID: 2240050 Review.

3

Diploid-triploid mosaicism: delineation of the syndrome.

Tharapel AT, Wilroy RS, Martens PR, Holbert JM, Summitt RL. Tharapel AT, et al. Ann Genet. 1983;26(4):229-33. Ann Genet. 1983. PMID: 6607703

4

Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus sampling.

Phillips OP, Tharapel AT, Lerner JL, Park VM, Wachtel SS, Shulman LP. Phillips OP, et al. Among authors: tharapel at. Am J Obstet Gynecol. 1996 Mar;174(3):850-5. doi: 10.1016/s0002-9378(96)70312-5. Am J Obstet Gynecol. 1996. PMID: 8633655 Review.

5

Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome.

Pivnick EK, Qumsiyeh MB, Tharapel AT, Summitt JB, Wilroy RS. Pivnick EK, et al. Among authors: tharapel at. J Med Genet. 1990 Aug;27(8):523-6. doi: 10.1136/jmg.27.8.523. J Med Genet. 1990. PMID: 2213846 Free PMC article. Review.

6

Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Pivnick EK, Velagaleti GV, Wilroy RS, Smith ME, Rose SR, Tipton RE, Tharapel AT. Pivnick EK, et al. Among authors: tharapel at. J Med Genet. 1996 Sep;33(9):772-8. doi: 10.1136/jmg.33.9.772. J Med Genet. 1996. PMID: 8880580 Free PMC article. Review.

7

46,XY monozygotic twins with discordant sex phenotype.

Somkuti SG, Wachtel SS, Schinfeld JS, Jackson L, Tharapel AT, DiGeorge AM. Somkuti SG, et al. Among authors: tharapel at. Fertil Steril. 2000 Dec;74(6):1254-6. doi: 10.1016/s0015-0282(00)01590-9. Fertil Steril. 2000. PMID: 11119763 Free article.

8

PRINS for mapping single-copy genes.

Tharapel AT, Wachtel SS. Tharapel AT, et al. Methods Mol Biol. 2006;338:59-67. doi: 10.1385/1-59745-097-9:59. Methods Mol Biol. 2006. PMID: 16888350

9

FISH and PRINS: competing or complementary technologies?

Wachtel SS, Tharapel AT. Wachtel SS, et al. Among authors: tharapel at. Am J Med Genet. 2002 Jan 15;107(2):97-8. doi: 10.1002/ajmg.10109. Am J Med Genet. 2002. PMID: 11807880 No abstract available.

10

Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement.

Tharapel AT, Redheendran R, Mankinen CB, Kukolich MK. Tharapel AT, et al. J Med Genet. 1984 Oct;21(5):391-5. doi: 10.1136/jmg.21.5.391. J Med Genet. 1984. PMID: 6239037 Free PMC article.

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