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Results: 1 to 20 of 27

PubMed Links for Books (Select 2981160)

1.

Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.

Littooij AS, Hochstenbach R, Sinke RJ, van Tintelen P, Giltay JC.

Am J Med Genet. 2002 Apr 22;109(2):125-32.

PMID:
11977161
2.

Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics.

Jalal SM, Law ME.

Genet Med. 1999 Jul-Aug;1(5):181-6.

PMID:
11256670
3.

De novo inverted duplication 9p21pter involving telomeric repeated sequences.

Sanlaville D, Baumann C, Lapierre JM, Romana S, Collot N, Cacheux V, Turleau C, Tachdjian G.

Am J Med Genet. 1999 Mar 12;83(2):125-31. Review.

PMID:
10190483
4.

Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.

Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G.

Ann Genet. 1998;41(3):133-40.

PMID:
9833066
5.

Segregation analysis of rare autosomal folate sensitive fragile sites.

Samadder P, Evans JA, Chudley AE.

Am J Med Genet. 1993 Apr 15;46(2):165-71.

PMID:
8484403
6.

Cutaneous malignant melanoma and atypical moles associated with a constitutional rearrangement of chromosomes 5 and 9.

Petty EM, Bolognia JL, Bale AE, Yang-Feng T.

Am J Med Genet. 1993 Jan 1;45(1):77-80.

PMID:
8418665
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8.

A female with XO/XY mosaicism and partial trisomy 9p.

Klasen M, Hansmann I, Schmid M, Schmidtke J.

J Med Genet. 1981 Dec;18(6):482. No abstract available.

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Expression of GALT in two unrelated 9p- patients. Evidence for assignment of the GALT locus to the 9p21 band.

Dagna Bricarelli F, Magnani M, Arslanian A, Camera G, Coviello DA, Di Pietro P, Dallapiccola B.

Hum Genet. 1981;59(2):112-4.

PMID:
6276288
13.

Chromosome studies in 952 infertile males with a sperm count below 10 million/ml.

Bourrouillou G, Dastugue N, Colombies P.

Hum Genet. 1985;71(4):366-7.

PMID:
4077053
14.

Maternal 3:1 disjunction in a translocation 9/17.

Sánchez Ferrer MA, de Torres ML, Abrisqueta JA.

Hum Genet. 1986 Jun;73(2):188. No abstract available.

PMID:
3721506
15.

Eleven new cases of del(9p) and features from 80 cases.

Huret JL, Leonard C, Forestier B, Rethoré MO, Lejeune J.

J Med Genet. 1988 Nov;25(11):741-9. Review.

17.

Genetic counseling in families with inherited balanced translocations: experience with 36 families.

Wolff G, Back E, Arleth S, Rapp-Körner U.

Clin Genet. 1989 Jun;35(6):404-16.

PMID:
2736789
18.

On the variable effect of mosaic normal/balanced chromosomal rearrangements in man.

Kleczkowska A, Fryns JP, Van den Berghe H.

J Med Genet. 1990 Aug;27(8):505-7. No abstract available.

19.

Four cases of trisomy 9p syndrome with particular chromosome rearrangements.

Bussani Mastellone C, Giovannucci Uzielli ML, Guarducci S, Nathan G.

Ann Genet. 1991;34(2):115-9.

PMID:
1746881
20.

Partial trisomy 17q and monosomy 9p due to a familial translocation.

Cotter PD, Stewart NL.

Ann Genet. 1990;33(4):231-3.

PMID:
1710432
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