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PMID: 4844639 Published · ppublish English Journal Article

Brother and sister with trisomy 10p: a new syndrome.

Humangenetik ·Vol. 23 ·No. 3 ·1974-00-00 ·Pages 163-72

Schleiermacher E, Schliebitz U, Steffens C

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/genetics Child Chromosome Aberrations Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Cleft Lip Cleft Palate Clubfoot Dermatoglyphics Face/abnormalities Female Humans Intellectual Disability/genetics Karyotyping Limb Deformities, Congenital Male Meiosis Pedigree Psychomotor Disorders/genetics Skull/abnormalities Syndrome Trisomy
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schleiermacher E
Schliebitz U
Steffens C
References (12)
12 references, click to expand
  1. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
    Ann Genet. 1970 Dec;13(4):217-32 PMID: 5313386
  2. Partial trisomy of 7q resulting from a familial translocation.
    Ann Genet. 1973 Mar;16(1):51-4 PMID: 4541809
  3. A rapid banding technique for routine use in human and comparative cytogenetics.
    Humangenetik. 1972;15(4):349-53 PMID: 4117698
  4. [Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation].
    Z Kinderheilkd. 1971;109(4):293-9 PMID: 5555168
  5. C8 trisomy mosaicism syndrome.
    Helv Paediatr Acta. 1972 Jul;27(3):281-98 PMID: 4645654
  6. Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.
    Humangenetik. 1971;12(3):175-81 PMID: 5563410
  7. [2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q].
    Ann Genet. 1972 Jun;15(2):85-92 PMID: 4537727
  8. A familial translocation t(6q+;8q-) identified by fluorescence microscopy.
    Humangenetik. 1973 Apr 16;18(2):189-92 PMID: 4737101
  9. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Humangenetik. 1973 Apr 16;18(2):129-38 PMID: 4124236
  10. [Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].
    Humangenetik. 1973;18(4):321-7 PMID: 4200006
  11. Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.
    J Med Genet. 1972 Mar;9(1):1-7 PMID: 4112567
  12. [Dominant hereditary perodactylia in 4 generations of a family; a phenogenetic study].
    Z Mensch Vererb Konstitutionsl. 1954;32(4):277-307 PMID: 13227282
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
DOI
10.1007/BF00285102
Published
1974-00-00
Pages
163-72
Language
English
Region
Germany
NLM ID
7607154
Subset
IM
External Links
PubMed source DOI: 10.1007/BF00285102
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