Kapur R - Search Results

1

Prenatal diagnosis of tetraploidy: a case report.

Coe SJ, Kapur R, Luthardt F, Rabinovitch P, Kramer D. Coe SJ, et al. Among authors: kapur r. Am J Med Genet. 1993 Feb 1;45(3):378-82. doi: 10.1002/ajmg.1320450320. Am J Med Genet. 1993. PMID: 8434628 Review.

2

Twin fetuses with abnormalities that overlap with three midline malformation complexes.

Hingorani SR, Pagon RA, Shepard TH, Kapur RP. Hingorani SR, et al. Among authors: kapur rp. Am J Med Genet. 1991 Nov 1;41(2):230-5. doi: 10.1002/ajmg.1320410220. Am J Med Genet. 1991. PMID: 1785640

3

Single umbilical artery. Prenatal detection of concurrent anomalies.

Nyberg DA, Mahony BS, Luthy D, Kapur R. Nyberg DA, et al. Among authors: kapur r. J Ultrasound Med. 1991 May;10(5):247-53. doi: 10.7863/jum.1991.10.5.247. J Ultrasound Med. 1991. PMID: 2051544

4

Azygous continuation of the interrupted inferior vena cava: a clue to prenatal diagnosis of the cardiosplenic syndromes.

Sheley RC, Nyberg DA, Kapur R. Sheley RC, et al. Among authors: kapur r. J Ultrasound Med. 1995 May;14(5):381-7. doi: 10.7863/jum.1995.14.5.381. J Ultrasound Med. 1995. PMID: 7609017

5

Diamniotic placentation associated with omphalopagus conjoined twins: implications for a contemporary model of conjoined twinning.

Kapur RP, Jack RM, Siebert JR. Kapur RP, et al. Am J Med Genet. 1994 Aug 15;52(2):188-95. doi: 10.1002/ajmg.1320520213. Am J Med Genet. 1994. PMID: 7802007

6

Trisomy 13 syndrome: prenatal US findings in a review of 33 cases.

Lehman CD, Nyberg DA, Winter TC 3rd, Kapur RP, Resta RG, Luthy DA. Lehman CD, et al. Among authors: kapur rp. Radiology. 1995 Jan;194(1):217-22. doi: 10.1148/radiology.194.1.7997556. Radiology. 1995. PMID: 7997556

7

Prenatal sonographic findings of trisomy 18: review of 47 cases.

Nyberg DA, Kramer D, Resta RG, Kapur R, Mahony BS, Luthy DA, Hickok D. Nyberg DA, et al. Among authors: kapur r. J Ultrasound Med. 1993 Feb;12(2):103-13. doi: 10.7863/jum.1993.12.2.103. J Ultrasound Med. 1993. PMID: 8468736

8

A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.

Nunes ME, Schutt G, Kapur RP, Luthardt F, Kukolich M, Byers P, Evans JP. Nunes ME, et al. Among authors: kapur rp. Hum Mol Genet. 1995 Nov;4(11):2165-70. doi: 10.1093/hmg/4.11.2165. Hum Mol Genet. 1995. PMID: 8589697

9

Follow-up of a familial translocation t(10;16) with an unusual segregation pattern.

Resta RG, Luthardt F, Kapur R. Resta RG, et al. Among authors: kapur r. Am J Med Genet. 1996 May 17;63(2):363-5. doi: 10.1002/(SICI)1096-8628(19960517)63:2<363::AID-AJMG7>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8725786

10

Trisomy 10p: report of an unusual mechanism of formation and critical evaluation of the clinical phenotype.

Clement SJ, Leppig KA, Jarvik GP, Kapur RP, Norwood TH. Clement SJ, et al. Among authors: kapur rp. Am J Med Genet. 1996 Oct 28;65(3):197-204. doi: 10.1002/(SICI)1096-8628(19961028)65:3<197::AID-AJMG5>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 9240743

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