(Q52089146)

22 April 2018

title

Excess of mental retardation and/or congenital malformation in reciprocal translocations in man. (English)

1 reference

22 April 2018

author name string

J P Fryns

1

1 reference

22 April 2018

A Kleczkowska

2

1 reference

22 April 2018

E Kubień

3

1 reference

22 April 2018

H Van den Berghe

4

1 reference

22 April 2018

publication date

1 January 1986

1 reference

22 April 2018

number of pages

8

1 reference

inferred from page(s)

published in

Human Genetics

1 reference

22 April 2018

volume

72

1 reference

22 April 2018

issue

1

1 reference

22 April 2018

page(s)

1-8

1 reference

22 April 2018

https://scigraph.springernature.com/pub.10.1007/bf00278808

exact match

0 references

cites work

Correlation between euploid structural chromosome rearrangements and mental subnormality in humans.

1 reference

12 December 2020

A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations

1 reference

12 December 2020

Chromosome abnormalities in newborn children. Physical aspects

1 reference

12 December 2020

Identification of translocation chromosomes by quinacrine fluorescence.

1 reference

12 December 2020

An analysis of the break points of structural rearrangements in man

1 reference

12 December 2020

Partial trisomy 1, karyotype 46,XY,12-,t(1q, 12p)+

1 reference

12 December 2020

Partial trisomy of chromosome 3(p14----p22) due to maternal insertional translocation

1 reference

12 December 2020

Autosomal reciprocal translocations and 13/14 translocations: a population study

1 reference

12 December 2020

Systematic analysis of 95 reciprocal translocations of autosomes

1 reference

12 December 2020

Distribution of spontaneous chromosome breaks in man

1 reference

12 December 2020

Partial trisomy 17q. Karyotype: 46,XY,der(21),t(17;21)(q22;p13).

1 reference

12 December 2020

De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy

1 reference

12 December 2020

Cytogenetic survey in couples with recurrent fetal wastage

1 reference

12 December 2020

Microfluorometric analysis of deoxyribonucleic acid replication kinetics and sister chromatid exchanges in human chromosomes

1 reference

12 December 2020

Constitutive fragile sites and cancer.

1 reference

12 December 2020

Trisomy of the short arm of chromosome number 9: a clinical entity

1 reference

12 December 2020

Partial trisomy 14q due to familial t(14q-,11q+) translocation

1 reference

12 December 2020

Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23

1 reference

12 December 2020

De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis

1 reference

12 December 2020

A malformed newborn with 9p and 4q trisomy

1 reference

12 December 2020

Possible excess of mental handicap and congenital malformations in autosomal reciprocal translocations

1 reference

12 December 2020

Partial trisomy 18q in a newborn with typical 18 trisomy phenotype

1 reference

12 December 2020

Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1

1 reference

12 December 2020

Balanced reciprocal translocations: risk factors for aneuploid segregant viability

1 reference

12 December 2020

Trisomy 12p due to familial t(12p-,6q plus) translocation.

1 reference

12 December 2020

Complex chromosomal rearrangements (CCR) and their genetic consequences.

1 reference

12 December 2020

New chromosomal syndromes. I. Partial trisomy of the distal portion of the long arm of chromosome number 10 (10q24 leads to 10qter): a clinical entity

1 reference

12 December 2020

Complex chromosomal rearrangement in a mentally retarded boy without gross dysmorphic stigmata.

1 reference

12 December 2020

Partial trisomy of the short arm of chromosome 3 (3p25 to 3pter). A distinct clinical entity

1 reference

12 December 2020

Familial partial distal 18q (18q22-18q23) trisomy

1 reference

12 December 2020

Partial trisomy 13: karyotype 46,XY,-6, plus t(13q,6q)

1 reference

12 December 2020

High-resolution chromosome analysis of phenotypically abnormal patients with apparently balanced structural rearrangements

1 reference

12 December 2020

Partial monosomy of the long arm of chromosome 16: A distinct clinical entity?

1 reference

12 December 2020

A cytogenetic survey of 11,680 newborn infants

1 reference

12 December 2020

Nonrandom distribution of exchange points in patients with reciprocal translocations

1 reference

12 December 2020

Mental retardation associated with "balanced" chromosome rearrangements

1 reference

12 December 2020

Myotonic dystrophy and autosomal balanced translocation t(2;20)(p21;q11)

1 reference

12 December 2020

Effect of balanced X/autosome translocations on sexual and physical development. A personal experience in 4 patients

1 reference

12 December 2020

Unusual translocation in Down syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00278808

1 reference

22 April 2018

1 reference

22 April 2018