Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States (Q35199625)

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English	Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States	scientific article

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2 October 2019

Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States (English)

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2 October 2019

recombinant 8 syndrome

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A C Smith

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2 October 2019

K Spuhler

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2 October 2019

T M Williams

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2 October 2019

T McConnell

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2 October 2019

E Sujansky

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2 October 2019

A Robinson

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2 October 2019

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1 December 1987

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2 October 2019

American Journal of Human Genetics

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2 October 2019

41

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2 October 2019

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2 October 2019

1083-1103

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3687942%20AND%20SRC:MED&resulttype=core&format=json

2 October 2019

Genetic tests under incomplete ascertainment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Spontaneous abortion over time: comparing occurrence in two cohorts of women a generation apart

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Structural differences in pericentric inversions. Application to a model of risk of recombinants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Pericentric inversion (13) with two different recombinants in the same family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Familial pericentric inversion of chromosome 13 resulting in duplication 13q22 to qter.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Experiences with unexpected structural chromosome aberrations in prenatal diagnosis in a Danish series

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Pericentric inversions. Problems and significance for clinical genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Familial pericentric inversion of chromosome 8.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Karyotype with chromosomal abnormality with various inherited defects in the offspring (Recombination aneusomy)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Outcome of pregnancies following a spontaneous abortion with chromosomal anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Pericentric inversions of human chromosomes 9 and 10.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Structural variation in chromosome No 9.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

An analysis of the break points of structural rearrangements in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Comments on methods and results in: Sherman et al., "Segregation analysis of balanced pericentric inversions in pedigree data".

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Segregation analysis of balanced pericentric inversions in pedigree data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Familial pericentric inversion of chromosome 12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Incidence of chromosome aberrations among 11 148 newborn children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

A large pericentric inversion of human chromosome 8

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 → 14qter)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Chromosome anomalies among livebirths

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Inversion homozygosity of chromosome no. 9 in a higly inbred kindred

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

Familial inversion of chromosome No. 8: an affected child and a carrier fetus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

13 July 2018

A child with recombinant of chromosome 8 inherited from a carrier mother with a pericentric inversion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684361

26 September 2018

A familial pericentric inversion of chromosome 8 analysed with a high resolution chromosome banding technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peri- and paracentric inversions in chromosome 12: prenatal diagnosis and family study

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unexpected structural chromosome rearrangements in prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated families

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinicopathologic and dysmorphic findings in recombinant chromosome 8 syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pericentric inversion of a group C autosome: a study of three families

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quinacrine Fluorescence Patterns and Terminal DNA Labelling of Human C Group Chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Q and C chromosomal variations: distribution and incidence

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pericentric inversion of chromosome No. 8

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surveillance of spontaneous abortions. Power in environmental monitoring

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A fetus with recombinant of chromosome 8 inherited from her carrier father

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome findings in 2,500 second trimester amniocenteses

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Chromosomal changes in evolution and in pathology: analysis of pericentric inversions]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic study of a large black kindred: inversions, heteromorphisms, and segregation analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?

1 reference

https://pubmed.ncbi.nlm.nih.gov/3687942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3687942%20AND%20SRC:MED&resulttype=core&format=json

2 October 2019

PubMed publication ID

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3687942%20AND%20SRC:MED&resulttype=core&format=json

2 October 2019

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