A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation.

Archives of disease in childhood ·Vol. 44 ·No. 233 ·1969-02-00 ·Pages 106-12

Thornburn MJ, Smith-Read EH, Peck JE

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/etiology Abortion, Habitual/etiology Adult Chromosome Aberrations Chromosome Disorders Chromosomes, Human, 4-5 Cytogenetics Female Humans Infant, Newborn Karyotyping Liver/pathology Male Mosaicism Phenotype Pregnancy

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Thornburn M J

Smith-Read E H

Peck J E

References (21)

21 references, click to expand

An asymmetric chromosome pair in group 4-5. Association with mental and physical retardation.
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A FAMILIAL 4/5 RECIPROCAL TRANSLOCATION RESULTING IN PARTIAL TRISOMY B.
Am J Hum Genet. 1965 Jan;17:54-70 PMID: 14255557
[On two familial cases of complex translocations].
Ann Genet. 1965;8(1):21-30 PMID: 5294577
Enlarged B-group chromosome (4-5). Association with the cri du chat syndrome.
Am J Dis Child. 1967 Feb;113(2):277-82 PMID: 6019447
PARTIAL AUTOSOMAL TRISOMY AND TRANSLOCATION. REPORT OF AN INFANT WITH MULTIPLE CONGENITAL ANOMALIES.
JAMA. 1964 Feb 22;187:566-9 PMID: 14089003
Pathology of congenital rubella in Jamaica.
Arch Dis Child. 1967 Aug;42(224):389-96 PMID: 4951637
[6-12 13-15 translocation and partial 6-12 trisomy (probably 10)].
Ann Genet. 1965;8(1):16-20 PMID: 5294576
Chromosome mosaicism in a child with features characteristic of the 'Cat Cry' syndrome.
J Med Genet. 1966 Mar;3(1):66-9 PMID: 5911836
Familial reciprocal C/18 translocation.
Am J Hum Genet. 1966 Nov;18(6):572-83 PMID: 5927877
Possible partial trisomy of a chromosome of group 6-X-12 and familial translocation heterozygosity in a child with congenital abnormalities.
Dev Med Child Neurol. 1967 Jun;9(3):313-8 PMID: 6035579
MATERNAL TRANSMISSION OF A NEW GROUP-C(6/9) CHROMOSOMAL SYNDROME.
Lancet. 1964 Oct 17;2(7364):838-40 PMID: 14197160
Translocation heterozygosis in man.
Am J Hum Genet. 1966 Mar;18(2):215-25 PMID: 5904864
An unstable ring chromosome in a female infant with hypotonia, seizures, and retarded development.
J Med Genet. 1966 Jun;3(2):134-8 PMID: 5963207
The costochondral junction during later stages of intrauterine life, and abnormal growth patterns found in association with perinatal death.
Arch Dis Child. 1967 Feb;42(221):1-13 PMID: 6066940
A simple method for short term cultures from small biopsies.
Exp Cell Res. 1963 Mar;30:229-32 PMID: 13969859
MICROTECHNIQUE FOR CULTURING LEUKOCYTES FROM WHOLE BLOOD.
Cytogenetics. 1963;2:57-60 PMID: 14099759
TRANSLOCATION IN THE 13-15 GROUP AS A CAUSE OF PARTIAL TRISOMY AND SPONTANEOUS ABORTION IN THE SAME FAMILY.
Lancet. 1963 Sep 14;2(7307):584-5 PMID: 14049598
Congenital anomalies due to transmission of a chromosome translocation.
J Med Genet. 1966 Mar;3(1):59-61 PMID: 5911833
A CASE OF PRIMARY AMENORRHEA WITH A TRANSLOCATION INVOLVING CHROMOSOMES OF GROUPS B AND C.
Am J Hum Genet. 1965 Sep;17:377-83 PMID: 14334736
A FAMILY APPARENTLY SHOWING TRANSMISSION OF A TRANSLOCATION BETWEEN CHROMOSOME 3 AND ONE OF THE 'X-6-12' OR 'C' GROUP.
J Med Genet. 1964 Sep;1(1):27-32 PMID: 14205979
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Article Info

Journal

Archives of disease in childhood

Abbr.

Arch Dis Child

ISSN

1468-2044

DOI

10.1136/adc.44.233.106

Published

1969-02-00

Pages

106-12

Language

English

Region

England

NLM ID

0372434

PMCID

PMC2020227

Subset

External Links

PubMed source DOI: 10.1136/adc.44.233.106 PMC Full Text View journal details

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A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation.

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