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Results: 15

PubMed Links for Books (Select 2983474)

1.

Multicolor spectral karyotyping of human chromosomes.

Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenksen D, Garini Y, Ried T.

Science. 1996 Jul 26;273(5274):494-7.

PMID:
8662537
2.

Clinical uses of computerized chromosome databases.

Borgaonkar DS.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:52-3. No abstract available.

PMID:
8629142
3.

Segregation analysis in reciprocal translocation carriers.

Petrosky DL, Borgaonkar DS.

Am J Med Genet. 1984 Sep;19(1):137-59.

PMID:
6496566
4.

Cytogenetic study of a 5-14 translocation in man.

Borgaonkar DS, Blair SM, Lutz JB, Kelly T, Tice RR, Delaney NV, Hutchinson JR, Bias WB.

J Hered. 1973 Sep-Oct;64(5):299-300. No abstract available.

PMID:
4782671
5.

Philadelphia-chromosome translocation and chronic myeloid leukaemia.

Borgaonkar DS.

Lancet. 1973 Jun 2;1(7814):1250. No abstract available.

PMID:
4122595
6.

Breakpoint distribution in constitutional chromosome rearrangements with respect to fragile sites.

Porfirio B, Dallapiccola B, Terrenato L.

Ann Hum Genet. 1987 Oct;51(Pt 4):329-36.

PMID:
3447515
7.

Prenatal diagnosis of tetrasomy 47,XY,+i(12p) confirmed by in situ hybridization.

Shivashankar L, Whitney E, Colmorgen G, Young T, Munshi G, Wilmoth D, Byrne K, Reeves G, Borgaonkar DS, Picciano SR, et al.

Prenat Diagn. 1988 Feb;8(2):85-91.

PMID:
3362782
8.

Familial ring (20) chromosomal mosaicism.

Back E, Voiculescu I, Brünger M, Wolff G.

Hum Genet. 1989 Sep;83(2):148-54.

PMID:
2777254
9.

A case of the ring 20 syndrome.

Thomsen SG, Petersen MB, Andersen EA, ostergaard GZ, Lindenberg S.

Ann Genet. 1989;32(2):111-3.

PMID:
2757359
10.

Chromosomal variation in man: catalog of chromosomal variants and anomalies.

Borgaonkar DS, Bolling DR, Partridge C, Ruddle FH, McKusick VA.

Birth Defects Orig Artic Ser. 1975;11(3):82-4. No abstract available.

PMID:
1203509
11.

Usefulness of chromosome catalog in delineating new syndromes.

Borgaonkar DS, Lacassie YE, Stoll C.

Birth Defects Orig Artic Ser. 1976;12(5):87-95. No abstract available.

PMID:
953248
12.

Usefulness of computerized data banks of human chromosomal variants and anomalies.

Borgaonkar DS, Bolling DR.

J Reprod Med. 1976 Jul;17(1):69-73. No abstract available.

PMID:
940088
13.

A (5;14) translocation, 46 chromosomes. Repository identification No. GM-589.

Borganonkar DS, Aronson MM, Greene AE, Coriell LL.

Cytogenet Cell Genet. 1977;18(4):242. No abstract available.

PMID:
872630
14.

Break points in human chromosomes.

Yu CW, Borgaonkar DS, Bolling DR.

Hum Hered. 1978;28(3):210-225.

PMID:
649178
15.

Order of genes for NP and TRPRS on chromosome 14.

Denney RM, Borgaonkar D, Ruddle FH.

Cytogenet Cell Genet. 1978;22(1-6):493-7. No abstract available.

PMID:
110526
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