S. Roberts

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Bilateral gynaecomastia as the sole presenting feature of a Y chromosome abnormality complicated by a gonadal tumour in an otherwise phenotypically normal male

P. Thompson, M. Scanlon, B. Issa, 1998 .

Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3

S. Davies, A. Meredith, S. Roberts, 1991, Journal of medical genetics.

Unbalanced reciprocal translocations in cases of Prader-Willi syndrome

P. Davies, S. Roberts, D. Duckett, 2004, Human Genetics.

The Cytogenetics of Mammalian Autosomal Rearrangements

S. Roberts, 1989 .

Rapid prenatal diagnosis of Patau's syndrome in a fetus with an abdominal wall defect by 72 hour culture of cells from amniotic fluid

M. Creasy, S. Roberts, Andrew J. Dawson, 1993, Prenatal diagnosis.

Adjacent 2 meiotic disjunction. Report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature

S. Roberts, D. Duckett, 1981, Human Genetics.

Outcome of fetuses with Turner syndrome: a 10-year congenital anomaly register based study

D. Tucker, M. Morgan, J. Matthes, 2012, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies.

A. Clarke, P. Harper, N. Thomas, 1986, Journal of medical genetics.

Trisomy l6p in a liveborn infant and a review of partial and full trisomy 16

S. Roberts, D. Duckett, 2022 .

Partial trisomy 12q: report of a case and review.

L. Pavone, T. Mattina, K. Laurence, 1981, Journal of medical genetics.

Intrachromosomal insertion of chromosome 13 in a family with psychosis and mental subnormality.

V. Cowie, S. Roberts, K. R. Singh, 2008, Journal of mental deficiency research.

Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome.

R. Snell, D. Shaw, P. Harper, 1991, Journal of medical genetics.

Assignment of human ferritin genes to chromosomes 11 and 19q13.3→19qter

M. Worwood, D. Shaw, J. Brook, 2004, Human Genetics.

Recurrent spontaneous abortions due to a homologous Robertsonian translocation (14q14q)

K. Laurence, S. Roberts, D. Duckett, 1982, Journal of medical genetics.

Double i(18q) in lymphoma.

K. Laurence, A. Mandal, S. Roberts, 1990, Cancer genetics and cytogenetics.

Duane syndrome associated with the Cat Eye syndrome: a case report

S. Roberts, D. Laws, T. Win, 2007, Eye.

Stable dicentric autosome, tdic (8:22)(p23:p13), in a mentally retarded girl.

R. Howell, K. Laurence, S. Roberts, 1977, Journal of medical genetics.

Further mapping of markers around the centromere of human chromosome 19.

D. Shaw, M. Skinner, J. Almond, 1987, Genomics.

Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness.

W. Reardon, N. S. Thomas, P. Phelps, 1992, American journal of medical genetics.

A cytogenetic deletion, del(17)(q11.22q21.1), in a patient with sporadic neurofibromatosis type 1 (NF1) associated with dysmorphism and developmental delay.

M. Upadhyaya, J. Maynard, P. Thompson, 1996, Journal of medical genetics.

A new DNA marker tightly linked to the fragile X locus (FRAXA).

K. Davies, P. Harper, D. Callen, 1989, Science.

Charcot-Marie-Tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2→12

J. Farnham, A. Clarke, P. Harper, 1993, Human Genetics.

Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm.

P. Harper, M. Upadhyaya, M. Sarfarazi, 1989, Journal of medical genetics.

The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments

J. S. Miles, S. Knight, D. Shaw, 2005, Human Genetics.

Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation.

P. Harper, J. Zonana, N. Thomas, 1988, Journal of medical genetics.

Newly described form of X-linked arthrogryposis maps to the long arm of the human X chromosome.

H. Houlden, M. Wallace, R. Zori, 1998, American journal of medical genetics.

Dicentric X isochromosomes in man.

R. Howell, S. Roberts, R. Beard, 1976, Journal of medical genetics.

Homozygous paracentric inversion 12 in a mentally retarded boy: a case report and review of the literature

K. Laurence, S. Roberts, H. Price, 1987, Human Genetics.

A new pericentric inversion of chromosome 6 in an abnormal infant.

S. Roberts, D. Duckett, 1980, Annales de genetique.

Replication studies in the 16p+ variant

P. Thompson, S. Roberts, S. Rees, 1990, Human Genetics.

A new variant of chromosome 16

P. Thompson, S. Roberts, 1987, Human Genetics.

Isochromosomes of both short and long arms of chromosome 12 resulting in an additional copy of chromosome 12 in a case of splenic lymphoma with villous lymphocytes.

P. Thompson, S. Roberts, S. M. Morgan, 1997, Cancer genetics and cytogenetics.

An improved lymphocyte culture technique: deoxycytidine release of a thymidine block and use of a constant humidity chamber for slide making.

R. Wheater, S. Roberts, 1987, Journal of medical genetics.