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Items: 1 to 20 of 27

2.

Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).

Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP.

Prenat Diagn. 2002 Jan;22(1):29-33.

PMID:
11810646
3.

Prenatal karyotyping using fetal blood obtained by cordocentesis: rapid and accurate results within 24 hours.

Tharapel SA, Dev VG, Shulman LP, Tharapel AT.

Ann Genet. 1998;41(2):69-72.

PMID:
9706335
4.

Genetic analysis by chromosome sorting and painting: phylogenetic and diagnostic applications.

Ferguson-Smith MA.

Eur J Hum Genet. 1997 Sep-Oct;5(5):253-65. Review.

PMID:
9412781
5.

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.

Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH.

Prenat Diagn. 1996 Jan;16(1):1-28.

PMID:
8821848
6.

Mosaicism with a normal cell line and an autosomal structural rearrangement.

Gardner RJ, Dockery HE, Fitzgerald PH, Parfitt RG, Romain DR, Scobie N, Shaw RL, Tumewu P, Watt AJ.

J Med Genet. 1994 Feb;31(2):108-14.

7.

Duplication of region 2q31 leads to 2qter in a family with 2/9 translocation.

Howard-Peebles PN, Goldsmith JP.

Hum Hered. 1980;30(2):84-8.

PMID:
7358400
8.

Interstitial deletion of the long arm of chromosome 2: case report and review of literature.

Taysi K, Dengler DR, Jones LA, Heersma JR.

Ann Genet. 1981;24(4):245-7. Review. No abstract available.

PMID:
7036843
9.

Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36).

Young RS, Shapiro SD, Hansen KL, Hine LK, Rainosek DE, Guerra FA.

J Med Genet. 1983 Jun;20(3):199-202.

10.

Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation.

Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M.

Hum Genet. 1983;64(1):98. No abstract available.

PMID:
6873945
11.

Interstitial deletion 2q31 leads to q33.

Buchanan PD, Rhodes RL, Stevenson CE Jr.

Am J Med Genet. 1983 May;15(1):121-6.

PMID:
6683075
12.

Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33).

Al-Awadi SA, Farag TI, Naguib K, Teebi A, Cuschieri A, Al-Othman S, Sundareshan TS.

J Med Genet. 1983 Dec;20(6):464-5.

13.

[Genetics of Patau's syndrome (an analysis of 59 families)].

Laziuk GI, Lur'e IV, Gurevich DB.

Tsitol Genet. 1984 Nov-Dec;18(6):453-4. Russian.

PMID:
6523569
14.
15.

Familial paracentric inversion inv(2)(q31q36).

Schmid M, Hofmann R, Köhler J, Jannek U.

Hum Genet. 1985;71(3):270-2.

PMID:
4065899
16.

Interstitial deletion of chromosome 2.

Marković S, Krstić M, Sulović V, Radojković Z, Adzić S.

J Med Genet. 1985 Apr;22(2):154-5. No abstract available.

17.

Localization of the human aryl hydrocarbon hydroxylase gene to the 2q31----2pter region of chromosome 2.

Ocraft KP, Muskett JM, Brown S.

Ann Hum Genet. 1985 Jul;49(Pt 3):237-9.

PMID:
3865622
18.
19.

A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.

Ramer JC, Ladda RL, Frankel CA, Beckford A.

Am J Med Genet. 1989 Mar;32(3):359-63. Review.

PMID:
2658585
20.

De novo complex chromosomal rearrangement in a woman with recurrent spontaneous abortion and one healthy daughter.

Timár L, Béres J, Kosztolányi G, Németh I.

Hum Genet. 1991 Feb;86(4):421.

PMID:
1999348

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