The 13q- deletion syndrome.

Journal of medical genetics ·Vol. 8 ·No. 3 ·1971-09-00 ·Pages 351-7

Grace E, Drennan J, Colver D, Gordon RR

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Analysis of Variance Autoradiography Chromosome Aberrations Chromosomes, Human, 13-15 Dermatoglyphics Female Humans Infant Karyotyping Leukocytes/cytology Male

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Grace E

Drennan J

Colver D

Gordon R R

References (17)

17 references, click to expand

Multiple congenital anomalies associated with a ring-D chromosome.
J Med Genet. 1969 Sep;6(3):314-21 PMID: 5345105
Retinoblastoma and deletion D (14) syndrome.
J Med Genet. 1969 Sep;6(3):322-7 PMID: 5345106
A ring D chromosome and anomalous inheritance of haptoglobin type.
J Pediatr. 1967 Feb;70(2):172-9 PMID: 6018104
Ring D1 chromosome and multiple malformations.
Lancet. 1969 Nov 8;2(7628):1009 PMID: 4186961
Chromosome abnormalities in two cases with bilateral radial element defects.
J Med Genet. 1969 Sep;6(3):342-6 PMID: 5345108
The Production of Homozygous Deficient Tissues with Mutant Characteristics by Means of the Aberrant Mitotic Behavior of Ring-Shaped Chromosomes.
Genetics. 1938 Jul;23(4):315-76 PMID: 17246891
Ring D chromosome: a second case associated with anomalous haptoglobin inheritance.
Science. 1967 Jun 30;156(3783):1746-8 PMID: 5611035
Absent thumbs with a ring D2 chromosome: a new deletion syndrome.
Am J Hum Genet. 1967 Sep;19(5):644-59 PMID: 6050738
The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study.
Cytogenetics. 1966;5(3):186-205 PMID: 5921499
[A case of D ring chromosome].
Ann Genet. 1969 Dec;12(4):259-61 PMID: 5309418
A human ring D chromosome associated with multiple congenital abnormalities.
J Pediatr. 1967 Jun;70(6):936-41 PMID: 6026119
Ring chromosomes in two infants with congenital malformations.
J Med Genet. 1969 Sep;6(3):334-41 PMID: 5345107
[The Dr phenotype: a study of threee cases with a ring D chromosome].
Ann Genet. 1968 Jun;11(2):79-87 PMID: 5303427
Multiple congenital abnormalities associated with ring chromosome.
Lancet. 1963 Aug 10;2(7302):304-5 PMID: 13969049
The 13q-deletion syndrome.
Am J Hum Genet. 1969 Sep;21(5):499-512 PMID: 5347076
CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.
Ann Hum Genet. 1963 Nov;27:171-4 PMID: 14081487
[Partial deletion of the long arm of a group D (13-15) chromosome :Dq-].
Ann Genet. 1967 Mar;10(1):25-31 PMID: 5300123

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

10.1136/jmg.8.3.351

Published

1971-09-00

Pages

351-7

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1469176

Subset

External Links

PubMed source DOI: 10.1136/jmg.8.3.351 PMC Full Text View journal details

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