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Items: 1 to 20 of 35

1.

Dilated ascending aorta in a child with ring chromosome 21 syndrome.

Rope AF, Hinton RB, Spicer RL, Blough-Pfau R, Saal HM.

Am J Med Genet A. 2004 Oct 1;130A(2):191-5.

PMID:
15372526
2.

Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism.

GRAY JE, MUTTON DE, ASHBY DW.

Lancet. 1962 Jan 6;1(7219):21-3. No abstract available.

PMID:
13901315
3.
4.

Molecular characterization of 21p- variant chromosome.

Conte RA, Mathews T, Kleyman SM, Verma RS.

Clin Genet. 1996 Aug;50(2):103-5.

PMID:
8937771
5.

Variant D and G-chromosomes in male-related infertility.

Moreau N, Teyssier M.

Arch Androl. 1982 Dec;9(4):307-10. No abstract available.

PMID:
7165411
6.
7.

A case of r(21) with stigmata of atypical Down syndrome.

Ieshima A, Ogasawara N, Yamamoto Y, Kuroki Y.

Hum Genet. 1980;55(1):65-9.

PMID:
6450156
8.

The origin of human trisomy: a study of heteromorphisms and satellite associations.

Jacobs PA, Mayer M.

Ann Hum Genet. 1981 Oct;45(Pt 4):357-65.

PMID:
6211127
9.

t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome.

Dallapiccola B, Bianco I, Brinchi V, Santulli B, Scarano G, Sicolo A, Stabile M, Ventruto V.

Ann Genet. 1982;25(1):56-8.

PMID:
6211124
10.

Maternally transmitted extra ring (21) chromosome in a boy with Down's syndrome.

Matsubara T, Nakagome Y, Ogasawara N, Oka S, Yokochi T.

Hum Genet. 1982;60(1):78-9. No abstract available.

PMID:
6210618
11.
12.

[21 p-maternal in duplicate in a case of trisomy 21].

de Grouchy J.

Ann Genet. 1970 Mar;13(1):52-5. French. No abstract available.

PMID:
5310106
13.

Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population.

Mikelsaar AV, Tüür SJ, Käosaar ME.

Humangenetik. 1973;20(2):89-101. No abstract available.

PMID:
4785172
14.

Elongated short arm of a G-group chromosome associated with similar phenotypic abnormalities in three patients.

Monteleone PL, Monteleone JA, Rivard D, Grzegocki JA.

J Pediatr. 1973 Sep;83(3):473-6. No abstract available.

PMID:
4725153
15.

Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II.

Magenis RE, Armendares S, Hecht F, Weleber RG, Overton K.

Ann Genet. 1972 Dec;15(4):265. No abstract available.

PMID:
4539485
16.

Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.

Warren RJ, Rimoin DL, Summitt RL.

Am J Hum Genet. 1973 Jan;25(1):77-81. No abstract available.

17.

46,XY,21qi-46,XY,21p- mosaicism in a child with Down's syndrome.

Atkins L, Feingold M.

J Med Genet. 1969 Jun;6(2):206-8. No abstract available.

18.

A case of a girl with a 21 ring chromosome.

Kucerová M, Polívková Z.

Hum Hered. 1974;24(1):100-4. No abstract available.

PMID:
4136482
19.

Frequency of deletion of short arm satellites in acrocentric chromosomes.

Nielsen J, Friedrich U, Hreidarsson AB.

J Med Genet. 1974 Jun;11(2):177-80. No abstract available.

20.

Prenatal karyotype analysis in high risk families.

Aula P, Karjalainen O.

Ann Clin Res. 1973 Jun;5(3):142-8. No abstract available.

PMID:
4127164

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