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Results: 9

PubMed Links for Books (Select 2983612)

1.

Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region.

Meins M, Hagh JK, Gerresheim F, Einhoff E, Olschewski H, Strehl H, Epplen JT.

Am J Med Genet A. 2005 Jan 1;132A(1):84-9.

PMID:
15551338
2.

Complex chromosomal translocation in a patient with Kallmann syndrome.

Kroisel PM, Petek E, Wagner K, Kurnik P.

Am J Med Genet. 2000 Mar 20;91(3):240. No abstract available.

PMID:
10756352
3.

Kleeblattschädel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24; q14).

McCorquodale M, Erickson RP, Robinson M, Roszczipka K.

Clin Genet. 1980 Jun;17(6):409-14.

PMID:
7398112
4.

Meiotic studies in two infertile males with autosomal translocations.

Mićić M, Mićić S.

Hum Genet. 1984;65(3):308-10.

PMID:
6698552
5.

Reproductive risks for translocation carriers: cytogenetic study and analysis of pregnancy outcome in 58 families.

Neri G, Serra A, Campana M, Tedeschi B.

Am J Med Genet. 1983 Dec;16(4):535-61.

PMID:
6660248
7.

Application of personal computer to an analysis of small de novo chromosomal insertion: a case of de novo 3q2 trisomy with ins(8;3).

Naritomi K, Izumikawa Y, Kinjo N, Miyagi C, Hirayama K.

Jinrui Idengaku Zasshi. 1989 Jun;34(2):113-21.

PMID:
2671451
8.

Fragile X testing in a diagnostic cytogenetics laboratory.

Voullaire LE, Webb GC, Leversha M.

J Med Genet. 1989 Jul;26(7):439-42.

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