Familial occurrence of a pseudodicentric chromosome 21

Case Reports

I Hancke et al. J Med Genet. 1985 Apr.

. 1985 Apr;22(2):155-6.

doi: 10.1136/jmg.22.2.155.

No abstract available

Similar articles

Analysis of banding patterns in a case of ring chromosome 21.
Richer CL, Fitch N, Sitahal S, Murer-Orlando M, Jean P. Richer CL, et al. Am J Med Genet. 1981;10(4):323-31. doi: 10.1002/ajmg.1320100404. Am J Med Genet. 1981. PMID: 7332027 No abstract available.
De novo partial monosomy 21 with unusual karyotype.
Al-Awadi SA, Naguib KK, Teebi AS, Sundareshan TS. Al-Awadi SA, et al. Jinrui Idengaku Zasshi. 1986 Mar;31(1):45-8. doi: 10.1007/BF01876801. Jinrui Idengaku Zasshi. 1986. PMID: 3735757 No abstract available.
Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome.
Kitsiou-Tzeli S, Hallett JJ, Atkins L, Latt SA, Holmes LB. Kitsiou-Tzeli S, et al. Am J Med Genet. 1984 Aug;18(4):725-9. doi: 10.1002/ajmg.1320180419. Am J Med Genet. 1984. PMID: 6237580
[Autosomal chromosome aberrations].
Schinzel A. Schinzel A. Arch Genet (Zur). 1979;52(1-2):1-204. Arch Genet (Zur). 1979. PMID: 389192 Review. German. No abstract available.
Chromosome 10qter deletion syndrome: a review and report of three new cases.
Wulfsberg EA, Weaver RP, Cunniff CM, Jones MC, Jones KL. Wulfsberg EA, et al. Am J Med Genet. 1989 Mar;32(3):364-7. doi: 10.1002/ajmg.1320320319. Am J Med Genet. 1989. PMID: 2658586 Review.