A. Berry

发表

Chromosomal Abnormalities in Dupuytren’s Contracture and Carpal Tunnel Syndrome

A. Bonnici, J. D. Spencer, S. P. Fox, 1992, Journal of hand surgery.

Prenatal recognition of 4p- syndrome.

C. Williams, M. Seller, A. Berry, 1977, Journal of medical genetics.

Rubinstein-Taybi syndrome.

A. Berry, Caroline Berry, 1987, Journal of medical genetics.

Monozygotic twins discordant for the oculo-oto-radial syndrome (IVIC syndrome).

N. Elçioglu, A. Berry, 1997, Genetic counseling.

Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.

C. Chantler, A. Berry, E. M. Belton, 1980, Journal of medical genetics.

FISH analysis in patients with clinical diagnosis of Williams syndrome *

N. Elçioglu, A. Berry, C. Mackie-Ogilvie, 1998, Acta paediatrica.

Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problems.

P. Benson, M. Seller, P. Polani, 1979, Journal of medical genetics.

A new form of autosomal dominant arthrogryposis.

J. Hall, A. Berry, M. Lai, 1991, Journal of medical genetics.

The use of non-metrical variations of the cranium in the study of Scandinavian population movements

A. Berry, 1974 .

Mosaicism and the trisomy 8 syndrome

D. Mutton, A. Berry, D. G. M. Lewis, 1978, Clinical genetics.

Chromosome deletion 17pl 1.2 (Smith‐Magenis syndrome) in seven new patients, four of whom had been referred for fragile‐X investigation

Z. Docherty, F. Behjati, M. Mullarkey, 1997, Clinical genetics.

A fetus with an X;1 balanced reciprocal translocation and eye disease.

S. Horsley, A. Davies, M. Seller, 1995, Journal of medical genetics.

Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasia.

J. Wilson, J. Griffin, C. Brain, 1998, Molecular endocrinology.

A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia.

J. Wilson, J. Griffin, C. Brain, 1995, Human molecular genetics.

Origins and relationships of the ancient Egyptians. Based on a study of non-metrical variations in the skull

R. Berry, A. Berry, 1972 .

Factors affecting the incidence of non-metrical skeletal variants.

A. Berry, 1975, Journal of anatomy.

XY sex-reversed campomelia

R. Trompeter, V. Shrubb, A. Berry, 1981, European Journal of Pediatrics.

The anthropological value of minor variants of the dental crown.

A. Berry, 1976, American journal of physical anthropology.

Two children with partial trisomy for 7p.

A. Berry, J. Honeycombe, S. Macoun, 1979, Journal of medical genetics.

Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndrome.

M. Bobrow, L. Zahed, J. Llerena, 1989, Journal of medical genetics.

Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism.

P. Scriven, A. Berry, C. Ball, 1992, Journal of medical genetics.

Two cases of interstitial deletion 1p.

M. Robards, A. Berry, C. Fear, 1991, Journal of medical genetics.

Chromosome 15 in floppy infants

B. Neville, A. Whittingham, A. Berry, 1981, Archives of disease in childhood.

Venous ulceration in males with sex chromosome abnormalities.

K. Burnand, S. Baker, A. Northeast, 1993, Journal of the Royal Society of Medicine.

CHROMOSOME 15 IN PRADER‐WILLI SYNDROME

D. Mutton, V. Dubowitz, J. Heckmatt, 1985, Developmental medicine and child neurology.

Syndrome of the month Tetrasomy 12p (Pallister-Killian syndrome)

A. Berry, 2022 .

Case Report: Partial trisomy of 15q due to inserted inverted duplication

A. Berry, C. Fear, N. Elçioğlu, 1997, Clinical genetics.

A child with partial monosomy 6q secondary to a maternal direct insertional event.

A. Berry, S. Matkins, J. Meyer, 1987, Journal of medical genetics.

Deletion of chromosome 3q proximal region gives rise to a variable phenotype

S. Hodgson, C. Ogilvie, A. Berry, 1998, Clinical genetics.

Chondrodysplasia punctata: another possible X-linked recessive case.

C. Bennett, M. Seller, D. Maxwell, 1992, American journal of medical genetics.

Two brothers with an unbalanced 8;17 translocation and infantile pyloric stenosis

S. Hodgson, S. Hodgson, A. Berry, 1995, Clinical genetics.

Prenatal diagnosis of a case of tetrasomy 9p

A. Fensom, A. Berry, S. Blunt, 1989, Prenatal diagnosis.

Prenatal diagnostic amniocentesis: problems with interpretation of unusual karyotypes

A. Berry, 1982 .

FISH analysis in patients with clinical diagnosis of Williams syndrome.

A. Berry, C. Mackie-Ogilvie, M. Daker, 1998 .

A case of malignant spinal cord ependymoma in association with a duplication of part of the long arm of chromosome 12.

B. Neville, A. Berry, Y. Stoddart, 1985, Journal of medical genetics.

Screening for Fragile X

A. Berry, 1997, Journal of medical screening.

The Genetics of Locomotor Disorders.

A. Berry, 1975 .

Triphalangeal thumb with delta phalanx in a case of Klinefelter's syndrome.

J. D. Spencer, J. D. Spencer, A. Berry, 1991, Journal of medical genetics.

Yunis-Varon syndrome with severe osteodysplasty.

C. Hall, C. Garrett, R. H. Simpson, 1990, Journal of medical genetics.

Predictive genetic testing in children.

A. Berry, 1996, Journal of medical genetics.

Familial transmission of a non‐Robertsonian translocation dicentric

P. Howard, A. Berry, 1986, Clinical genetics.