S. Youings

发表

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

P. Jacobs, A. Cockwell, M. Mackenzie, 1991, Journal of medical genetics.

An Investigation of FRAXA Intermediate Allele Phenotype in A Longitudinal Sample

N. Morton, S. Ring, M. Pembrey, 2006, Annals of human genetics.

The efficacy of maternal age screening for Down's syndrome in Wessex

P. Jacobs, S. Youings, N. Gregson, 1991, Prenatal diagnosis.

Failure to find DUP25 in patients with anxiety disorders, in control individuals, or in previously reported positive control cell lines

J. Crolla, P. Jacobs, D. Baldwin, 2003 .

P.3.033 Failure to find DUP25 in patients with anxiety disorders, in control individuals, or in previously reported positive control cell lines

J. Crolla, P. Jacobs, D. Baldwin, 2003, European Neuropsychopharmacology.

Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man

N. S. Thomas, P. Jacobs, M. Durkie, 2006, Human Genetics.

Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.

P. Jacobs, A. Murray, S. Youings, 1996, Human molecular genetics.

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation.

P. Jacobs, S. Youings, J. Macpherson, 1994, Human molecular genetics.

FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability.

N. Morton, P. Jacobs, A. Murray, 1998, Proceedings of the National Academy of Sciences of the United States of America.

A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions

N. S. Thomas, P. Jacobs, K. Lachlan, 2005, Human Genetics.

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

J. Crolla, P. Jacobs, P. Betts, 1990, Annals of human genetics.

A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities

J. Barber, P. Jacobs, S. Ennis, 2004, American journal of medical genetics. Part A.

Mortality and cancer incidence in persons with numerical sex chromosome abnormalities: a cohort study

V. Beral, A. Swerdlow, P. Jacobs, 2001 .

Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11

R. Sandford, N. S. Thomas, P. Jacobs, 2006, European Journal of Human Genetics.

Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited

J. Crolla, P. Jacobs, S. Ennis, 2005, European Journal of Human Genetics.

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes

N. Carter, R. Sandstrom, H. Fiegler, 2005, Journal of Medical Genetics.

Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders

P. Bolton, N. S. Thomas, E. Weisblatt, 2004, Psychiatric genetics.

Population studies of the fragile X: a molecular approach.

P. Jacobs, S. Youings, A. Watson, 1993, Journal of medical genetics.

FRAXA and FRAXE: the results of a five year survey

P. Jacobs, A. Murray, S. Ennis, 2000, Journal of medical genetics.

The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission.

N. Morton, P. Jacobs, A. Murray, 1997, Human Molecular Genetics.

Stability and haplotype analysis of the FRAXE region

N. Morton, P. Jacobs, A. Murray, 2000, European Journal of Human Genetics.

A cytogenetic andmolecular study ofa series of45,X fetuses andtheir parents

P. Jacobs, A. Cockwell, S. Youings, 2017 .