Format
Sort by
Items per page

Send to

Choose Destination

Links from Books

Items: 19

1.

Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21.

Brisset S, Aboura A, Audibert F, Costa JM, L'Herminé AC, Gautier V, Frydman R, Tachdjian G.

Prenat Diagn. 2003 Jun;23(6):461-9.

PMID:
12813759
2.

A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21.

Ilgin Ruhi H, Tükün A, Karabulut H, Bayazit P, Bökesoy I.

Clin Genet. 2001 May;59(5):368-70. No abstract available.

PMID:
11359472
3.

Mosaicism for a small marker chromosome resulting from a familial Robertsonian translocation (21;22).

Arab S, Chitayat D, Gardner HA, Winsor EJ.

Clin Genet. 1999 Nov;56(5):362-6.

PMID:
10668926
4.
5.
6.

Chromosome abnormalities in congenital heart disease.

Johnson MC, Hing A, Wood MK, Watson MS.

Am J Med Genet. 1997 Jun 13;70(3):292-8.

PMID:
9188669
7.

Confirmation of Down syndrome critical region by FISH analysis in a patient with add(21) (p11)

Matsumoto N, Niikawa N, Mikawa M.

Am J Med Genet. 1995 Dec 4;59(4):521-2. No abstract available.

PMID:
8585576
8.

Lens dislocation and optic nerve hypoplasia in ring chromosome 21 mosaicism.

Meire FM, Fryns JP.

Ann Genet. 1994;37(3):150-2.

PMID:
7847798
9.

Three new cases of partial monosomy 21 resulting from one ring 21 chromosome and two unbalanced reciprocal translocations.

Philip N, Baeteman MA, Mattei MG, Mattei JF.

Eur J Pediatr. 1984 Apr;142(1):61-4.

PMID:
6714262
10.

Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation.

Cantu JM, Hernandez A, Plascencia L, Vaca G, Moller M, Rivera H.

Ann Genet. 1980;23(3):183-6.

PMID:
6448566
11.

Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and Italy.

Schmid W, Tenconi R, Baccichetti C, Caufin D, Schinzel A.

Am J Med Genet. 1983 Nov;16(3):323-9.

PMID:
6228144
12.

Human autosomal deletion mapping and HL-A.

Kreiger D, Palmer C, Biegel A.

Humangenetik. 1974 Jul 15;23(2):159-60. No abstract available.

PMID:
4852303
13.

Dicentric and monocentric Robertsonian translocations in man.

Niebuhr E.

Humangenetik. 1972;16(3):217-26. No abstract available.

PMID:
4117153
14.

Ring chromosome 21 in a phenotypically normal but infertile man.

Huret JL, Leonard C, Kanoui V.

Clin Genet. 1985 Dec;28(6):541-5.

PMID:
4075565
15.

In situ hybridization and translocation breakpoint mapping. II. Two unusual t(21;22) translocations.

Cannizzaro LA, Aronson MM, Emanuel BS.

Cytogenet Cell Genet. 1985;39(3):173-8.

PMID:
3930156
16.

Two Down syndrome patients with rec(21),dupq,inv(21)(p11;q2109) from a familial pericentric inversion.

Léonard C, Gautier M, Sinet PM, Selva J, Huret JL.

Ann Genet. 1986;29(3):181-3.

PMID:
2947534
17.

Familial transmission of a ring chromosome 21.

Hertz JM.

Clin Genet. 1987 Jul;32(1):35-9.

PMID:
2887318
18.

Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype.

Krasikov N, Takaesu N, Hassold T, Knops JF, Finley WH, Scarbrough P.

Am J Med Genet. 1992 Jun 1;43(3):554-60.

PMID:
1605248
19.

Human acrocentric ring chromosomes and satellite association.

Cantu JM, Salamanca F, Sanchez J, Peña T, Pacheco C, Armendares S.

Ann Genet. 1975 Sep;18(3):193-6.

PMID:
1080983

Supplemental Content

Support Center