(Q29030151)

26 March 2017

1 reference

1 reference

Nancy Monroy

1

1 reference

26 March 2017

Marisol López

2

1 reference

26 March 2017

Alicia Cervantes

3

1 reference

26 March 2017

Diana García-Cruz

4

1 reference

26 March 2017

Gildardo Zafra

5

1 reference

26 March 2017

Sonia Canún

6

1 reference

26 March 2017

Juan Carlos Zenteno

7

1 reference

26 March 2017

Susana Kofman-Alfaro

8

1 reference

26 March 2017

publication date

10 December 2001

1 reference

American Journal of Medical Genetics Part A

26 March 2017

published in

1 reference

26 March 2017

volume

107

1 reference

26 March 2017

page(s)

181-189

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26 March 2017

issue

3

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On the parental origin of de novo mutation in man.

26 March 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Possible role of imprinting in the Turner phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

A cytogenetic and molecular study of a series of 45,X fetuses and their parents

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

A comparison of the clinical and cytogenetic findings in nine patients with a ring (X) cell line and 16 45,X patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Three patients with a 45,X/46,X,psu dic(Xp) karyotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Three patients with ring (X) chromosomes and a severe phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Turner syndrome: a study of chromosomal mosaicism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Analysis of sex chromosome aneuploidy in 41 patients with Turner syndrome: a study of 'hidden' mosaicism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Molecular diagnosis of Turner's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Non-disjunction in human sperm: evidence for an effect of increasing paternal age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Molecular studies of parental origin and mosaicism in 45,X conceptuses

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Counting cross-overs: characterizing meiotic recombination in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Turner syndrome: a cytogenetic and molecular study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Frequency of Y chromosomal material in Mexican patients with Ullrich-Turner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Analysis of the origin of Turner's syndrome using polymorphic DNA probes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Capillary electrophoresis of DNA for molecular diagnostics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Stable dicentric X chromosomes with two functional centromeres.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Parental origin of the X chromosome, X chromosome mosaicism and screening for “hidden” Y chromosome in 45,X Turner syndrome ascertained cytogenetically

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Molecular studies of the parental origin and nature of human X isochromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Molecular study of 45,X conceptuses: correlation with clinical findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

A study of 45,X/46,XX mosaicism in Turner syndrome females: a novel primer pair for the (CAG)n repeat within the androgen receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

PCR Protocol to Detect Parental Origin and Hidden Mosaicism inSex Chromosome Aneuploidies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Analysis of sex chromosome aneuploidy in sperm from fathers of Turner syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Paternal sex chromosome aneuploidy as a possible origin of Turner syndrome in monozygotic twins: Case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

High frequency of tissue-specific mosaicism in Turner syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Dicentric chromosomes and the inactivation of the centromere

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

PCR-based detection of mosaicism in Turner syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10113

21 January 2018

Identifiers

DOI

10.1002/AJMG.10113

1 reference