Partial trisomy 10q - A recognizable syndrome

Human Genetics

Volumn 46, Issue 1, 1979, Pages 29-40

  Klep de Pater, Johanna M ^a   Bijlsma, Jan B ^b   de France, Henny F ^b   Leschot, Nico J ^b   Duijndam van den Berge, Mia ^c   van Hemel, Jan O ^d  

^a Observation Clinic De Ederhorst ^*  (Netherlands)

^b UNIVERSITY OF AMSTERDAM   (Netherlands)

^c Psychiatric Hospital Endegeest   (Netherlands)

^d UTRECHT UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CENTRAL NERVOUS SYSTEM; CHROMOSOME 10Q; CHROMOSOME TRANSLOCATION 10; CHROMOSOME TRANSLOCATION 17; CONGENITAL DISORDER; CONGENITAL MALFORMATION; CYTOLOGY; DIAGNOSIS; FACE DYSMORPHIA; GROWTH RETARDATION; HEREDITY; HISTOLOGY; MENTAL DEFICIENCY; MENTAL RETARDATION MALFORMATION SYNDROME; PARTIAL TRISOMY 10; SYNDROME DELINEATION;

ADOLESCENT; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, 6-12 AND X; DERMATOGLYPHICS; FACE; FEMALE; GROWTH DISORDERS; HUMANS; KARYOTYPING; MALE; MENTAL RETARDATION; MIDDLE AGED; PEDIGREE; PHENOTYPE; SYNDROME; TRISOMY;

EID: 0018292097     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00278899     Document Type: Article

References (19)

1. Trisomie 10q partielle de novo
2. Inversion péricentrique, inv(10), chez la mère et aneusomie de recombinaison, inv(10),rec(10), chez son fils
3. Trisomy of the distal third of the long arm of chromosome 10. Report of a new case due to a familial translocation t(10;18) (q24;p11)
4. Deux nouveaux cas de trisomie 10q24→ 10qter chez deux soeurs par translocation paternelle t(9;10)(q34;q24)
5. Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations
6. An improved banding technique examplified in the karyotype analysis of two strains of rat
7. Deux translocations familiales survenues ensemble chez chacune de deux soeurs, l'une équilibrée, l'autre trisomique partielle 10q
8. Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23)
9. Trisomie 10 partielle par translocation familiale t(1;10)(q44;q22)
10. Familial partial trisomy of the long arm of chromosome 10 (q24–26)
11. A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation
12. La trisomie 10q24→10qter
13. Ocular phenotype in partial trisomy 10q
14. Sclerocornea with an unbalanced translocation (17p,10q)
15. Trisomie partielle 10q par translocation familiale t(10q-;22p+)
16. A simple method for R-banding of human chromosomes showing a pH-dependent connection between R- and G-bands
17. Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q
18. Inherited translocations in two families [t(14q+;10q-) and t(13q-;21q+)]
19. A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10