Format
Sort by
Items per page

Send to

Choose Destination

Links from Books

Items: 1 to 20 of 30

1.

De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder.

Lespinasse J, Bugge M, Réthoré MO, North MO, Lundsteen C, Kirchhoff M.

Am J Med Genet A. 2004 Jul 15;128A(2):199-203.

PMID:
15214017
2.

High resolution comparative genomic hybridisation in clinical cytogenetics.

Kirchhoff M, Rose H, Lundsteen C.

J Med Genet. 2001 Nov;38(11):740-4.

3.

Clinical applications of comparative genomic hybridization.

Levy B, Dunn TM, Kaffe S, Kardon N, Hirschhorn K.

Genet Med. 1998 Nov-Dec;1(1):4-12.

PMID:
11261428
4.

Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy.

Anderlid BM, Sahlén S, Schoumans J, Holmberg E, Ahsgren I, Mortier G, Speleman F, Blennow E.

Am J Med Genet. 2001 Mar 15;99(3):223-33.

PMID:
11241494
5.

A new method for detecting pericentric inversions using COD-FISH.

Bailey SM, Meyne J, Cornforth MN, McConnell TS, Goodwin EH.

Cytogenet Cell Genet. 1996;75(4):248-53.

PMID:
9067435
6.

Familial pericentric inversion incidentally detected at prenatal diagnosis.

Uehara S, Takabayashi T, Takeyama Y, Okamura K, Yajima A.

Jpn J Hum Genet. 1995 Sep;40(3):259-63.

PMID:
8527800
7.

[Holt-Oram syndrome in combination with reciprocal translocation, lung hypoplasia and cardiomyopathy].

Kullmann F, Koch R, Feichtinger W, Giesen H, Schmid M, Grimm T.

Klin Padiatr. 1993 May-Jun;205(3):185-9. German.

PMID:
8350593
8.

Interstitial deletion in chromosome 1: assignment of the breakpoints.

Köhler A.

Am J Med Genet. 1993 Nov 15;47(7):1144-5. No abstract available.

PMID:
8291536
9.

"Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents.

Wenger SL, Steele MW, Boone LY, Lenkey SG, Cummins JH, Chen XQ.

Am J Med Genet. 1995 Jan 2;55(1):47-52.

PMID:
7702096
10.

Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.

Chen H, Tuck-Muller CM, Batista DA, Wertelecki W.

Am J Med Genet. 1995 Mar 27;56(2):219-33. Review.

PMID:
7625449
11.

[Maternal translocation t (1; 8; 15) and trisomy 8 qter in her daughter. Genetic counseling].

Ballesta F, Fernández E, Milá M.

J Genet Hum. 1980 Sep;28(3):361-6. French. No abstract available.

PMID:
7463035
12.

Pericentric inversion of chromosome 1 in three sterile brothers.

Giraldo A, Silva E, Martínez I, Campos C, Guzmán J.

Hum Genet. 1981;58(2):226-7. No abstract available.

PMID:
7287009
13.
14.

Pericentric inversions. Problems and significance for clinical genetics.

Kaiser P.

Hum Genet. 1984;68(1):1-47. Review.

PMID:
6389316
15.

Position of the Duffy locus on chromosome 1 in relation to breakpoints for structural rearrangements.

Lee CS, Ying KL, Bowen P.

Am J Hum Genet. 1974 Jan;26(1):93-102. No abstract available.

16.

An analysis of the break points of structural rearrangements in man.

Jacobs PA, Buckton KE, Cunningham C, Newton M.

J Med Genet. 1974 Mar;11(1):50-64. No abstract available.

17.

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
18.

Chromosome studies of 500 couples with two or more abortions.

Sachs ES, Jahoda MG, Van Hemel JO, Hoogeboom AJ, Sandkuyl LA.

Obstet Gynecol. 1985 Mar;65(3):375-8.

PMID:
3974963
19.

Segregation analysis of balanced pericentric inversions in pedigree data.

Sherman SL, Iselius L, Gallano P, Buckton K, Collyer S, DeMey R, Kristoffersson U, Lindsten J, Mikkelsen M, Morton NE, et al.

Clin Genet. 1986 Aug;30(2):87-94.

PMID:
3757307
20.

Supplemental Content

Support Center