Format
Items per page
Sort by

Send to:

Choose Destination

Results: 19

PubMed Links for Books (Select 2981150)

1.

DNA replication-timing analysis of human chromosome 22 at high resolution and different developmental states.

White EJ, Emanuelsson O, Scalzo D, Royce T, Kosak S, Oakeley EJ, Weissman S, Gerstein M, Groudine M, Snyder M, Schübeler D.

Proc Natl Acad Sci U S A. 2004 Dec 21;101(51):17771-6. Epub 2004 Dec 10.

2.

Severe intra-uterine growth retardation in a patient with maternal uniparental disomy 22 and a 22-trisomic placenta.

Balmer D, Baumer A, Röthlisberger B, Schinzel A.

Prenat Diagn. 1999 Nov;19(11):1061-4.

PMID:
10589061
3.

Prenatal diagnosis of an extranumerary i(22p) with normal phenotype.

Doneda L, Dalprà L, Tibiletti MG, Larizza L.

Ann Genet. 1993;36(3):154-8.

PMID:
8117060
4.

Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children.

Gravholt CH, Friedrich U.

Am J Med Genet. 1995 Mar 13;56(1):106-11. Review.

PMID:
7747772
5.

Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter.

Palmer CG, Schwartz S, Hodes ME.

Clin Genet. 1980 Jun;17(6):418-22.

PMID:
7398113
6.

Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22.

Geurts van Kessel AH, Westerveld A, de Groot PG, Meera Khan P, Hagemeijer A.

Cytogenet Cell Genet. 1980;28(3):169-72.

PMID:
7192199
7.

Identification of 21r and 22r chromosomes by quinacrine fluorescence.

Crandall BF, Weber F, Muller HM, Burwell JK.

Clin Genet. 1972;3(4):264-70. No abstract available.

PMID:
5054320
8.

Chromosomal abnormality associated with congenital macroglossia and other abnormalities.

Smith GF, Sachdeva S, Janakiraman N, Sinha SN.

J Med Genet. 1974 Dec;11(4):406-10. No abstract available.

9.

Human chromosome 22.

Kaplan JC, Aurias A, Julier C, Prieur M, Szajnert MF.

J Med Genet. 1987 Feb;24(2):65-78. Review.

10.

Parental origin of the extra chromosome in the cat eye syndrome: evidence from heteromorphism and in situ hybridization analysis.

Magenis RE, Sheehy RR, Brown MG, McDermid HE, White BN, Zonana J, Weleber R.

Am J Med Genet. 1988 Jan;29(1):9-19.

PMID:
3344779
11.

Placental mosaicism in a case of 46,XY,-22,+t(22;22)(p11;q11) or i(22q) diagnosed at amniocentesis.

Spinner NB, Gibas Z, Kline R, Berger B, Jackson L.

Prenat Diagn. 1992 Jan;12(1):47-51.

PMID:
1557310
12.
13.

Prenatal identification of small mosaic markers of different chromosomal origins.

Stetten G, Blakemore KJ, Courter AM, Coss CA, Jabs EW.

Prenat Diagn. 1992 Feb;12(2):83-91.

PMID:
1372733
14.

A 22/22 translocation carrier with recurrent abortions demonstrated by a Giemsa banding technique,.

Maeda T, Ohno M, Shimada N, Nishida M, Jobo T.

Hum Genet. 1976 Feb 29;31(2):243-5.

PMID:
1248834
15.

Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortions.

Farah LM, de Nazareth HR, Dolnikoff M, Delascio D.

Humangenetik. 1975 Aug 25;28(4):357-60. No abstract available.

PMID:
1176128
16.

Assignment of the DIA1 locus to chromosome 22.

Fisher RA, Povey S, Bobrow M, Solomon E, Boyd Y, Carritt B.

Ann Hum Genet. 1977 Oct;41(2):151-5.

PMID:
596823
17.

A further case of a 22;22 Robertsonian translocation associated with recurrent abortions.

Mameli M, Cardia S, Milia A, Seabright M.

Hum Genet. 1978 Apr 24;41(3):359-61.

PMID:
565744
19.

Partial trisomy 22q with elevated arylsulfatase-A activity.

Fryns JP, Jaeken J, van den Berghe H.

Ann Genet. 1979;22(3):168-70.

PMID:
43111
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk