214 related articles for article (PubMed ID: 4255306)
1. Chromosome 16 heterology. Nonspecific variation in karyotype?
Kelly S; Almy R
N Y State J Med; 1971 Oct; 71(19):2297-9. PubMed ID: 4255306
[No Abstract] [Full Text] [Related]
2. Chromosomal analysis in some cases of mental and physical defects in children.
Khandelwal MK; Jaiswal RB; Solanki BR; Grover S
Indian Pediatr; 1968 Mar; 5(3):100-6. PubMed ID: 4234583
[No Abstract] [Full Text] [Related]
3. Incidence of chromosomal abnormalities in the institutionalised mental retardates.
Roy I; Seth PK; Seth S
Indian Pediatr; 1979 Oct; 16(10):855-9. PubMed ID: 161287
[No Abstract] [Full Text] [Related]
4. [The intelligence level in the chromosome aberrations affecting autosomes].
Moor L
Rev Neuropsychiatr Infant; 1970 Dec; 18(12):943-66. PubMed ID: 4251821
[No Abstract] [Full Text] [Related]
5. Structural variation in human nitotic chromosomes.
Leisti J
Ann Acad Sci Fenn Biol; 1971; 179():1-69. PubMed ID: 4261167
[No Abstract] [Full Text] [Related]
6. [Peculiar findings in G group chromosome aberrations].
Grünwald P; Schweikhardt F
Acta Genet Med Gemellol (Roma); 1969 Jan; 18(1):92-8. PubMed ID: 4240534
[No Abstract] [Full Text] [Related]
7. [Genetic studies in severe mental retardation].
Cholnoky P; Méhes K; Sulyok E; Farkas G; Major L
Orv Hetil; 1968 Apr; 109(15):809-14. PubMed ID: 4236500
[No Abstract] [Full Text] [Related]
8. The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).
Parker CE; Mavalwala J; Koch R; Hatashita A; Derencsenyi A
Calif Med; 1972 Oct; 117(4):65-71. PubMed ID: 5075725
[No Abstract] [Full Text] [Related]
9. Cardio-facio-cutaneous (CFC) syndrome in a child carrying an inherited inversion of chromosome 7.
Lopez-Rangel E; Hrynchak M; Friedman JM
Am J Med Genet; 1993 Sep; 47(3):326-9. PubMed ID: 8135275
[TBL] [Abstract][Full Text] [Related]
10. [Chromosomal mosaicism in the r (15) syndrome].
Malygina NA; Mutovin GR; Filina NP; Akif'ev AP
Genetika; 1980; 16(11):2029-33. PubMed ID: 7193157
[TBL] [Abstract][Full Text] [Related]
11. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
[No Abstract] [Full Text] [Related]
12. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
Taysi K; Dengler DR; Jones LA; Heersma JR
Ann Genet; 1981; 24(4):245-7. PubMed ID: 7036843
[No Abstract] [Full Text] [Related]
13. [Cytogenetic studies in clinical diagnosis --analysis of 1611 examination results].
Bocian E; Mazurczak T; Stańczak H
Przegl Lek; 1995; 52(1):5-9. PubMed ID: 7784612
[TBL] [Abstract][Full Text] [Related]
14. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].
Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B
Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122
[No Abstract] [Full Text] [Related]
15. [Signs of developmental dysplasia and function of the genetic apparatus of children and adolescents].
Sitnikov VF; Khardikov AA; Morozov NN
Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(3):35-9. PubMed ID: 2968030
[TBL] [Abstract][Full Text] [Related]
16. [Chromosome aberration and mental retardation].
Asaka A
Shinkei Kenkyu No Shimpo; 1972 Apr; 16(2):226-31. PubMed ID: 4260444
[No Abstract] [Full Text] [Related]
17. [Cytogenetic studies of families of patients with Down's syndrome].
Davidenkova EF; Kolosova NN; Pantova IG; Shushval ON
Tsitologiia; 1966; 8(2):277-82. PubMed ID: 4228480
[No Abstract] [Full Text] [Related]
18. Partial deletion of long arms of chromosome 18.
Kushnick T; Matsushita G
Pediatrics; 1968 Jul; 42(1):194-7. PubMed ID: 5657675
[No Abstract] [Full Text] [Related]
19. Genetics for the cardiologist. Part II: Chromosomal and polygenic inheritance and genetic counseling.
Rowley PT
Mod Concepts Cardiovasc Dis; 1978 Feb; 47(2):67-70. PubMed ID: 147405
[No Abstract] [Full Text] [Related]
20. [A patient with ring chromosome 13].
Hammond A; Bijlsma JB
Ned Tijdschr Geneeskd; 1981 May; 125(19):752-5. PubMed ID: 7242723
[No Abstract] [Full Text] [Related]
[Next] [New Search]
