M. Ridler

发表

Red cell size and uric acid in Down's syndrome.

A. Howell, A. Mason, E. Brown, 2009, Scandinavian journal of haematology.

Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities.

M. Ridler, M. Liberman, M. Crawfurd, 1979, Journal of medical genetics.

PRESENILE DEMENTIA ASSOCIATED WITH MOSAIC TRISOMY 21 IN A PATIENT WITH A DOWN SYNDROME CHILD

M. Ridler, F. Gibberd, I. Rowe, 1989, The Lancet.

A diagnostic survey of infants referred for chromosome analysis in the neonatal period.

R. Winter, M. Ridler, J. McKeown, 1980, British medical journal.

An etiological survey of the severely retarded Hertfordshire children who were born between January 1, 1965 and December 31, 1967.

J. Opitz, R. Laxová, M. Ridler, 1977, American journal of medical genetics.

A case of a paracentric inversion inv(7)(q11q22). Prenatal detection and counselling

M. Ridler, S. Sutton, Michael A. C. Ridler, 1981, Prenatal diagnosis.

An aetiological study of fifty-three female patients from a subnormality hospital and of their offspring.

R. Laxová, M. Ridler, S. Gilderdale, 2008, Journal of mental deficiency research.

Family with probable achondrogenesis and lipid inclusions in fibroblasts

R. Laxová, M. Ridler, P. Ohara, 1973, Archives of disease in childhood.

Action of Cytochalasin B on Cultured Human Lymphocytes

M. Ridler, G. Smith, J. Faunch, 1967, Nature.

The chromosomes in a patient showing both mongolism and the Klinefelter syndrome.

L S PENROSE, C. E. Ford, L. Penrose, 1959, Lancet.

The response of human cultured lymphocytes to cytochalasin B.

M. Ridler, G. Smith, 1968, Journal of cell science.

Familial transmission of an aberrant submetacentric chromosome.

M. Ridler, G. F. Smith, J. M. Berg, 2008, Journal of mental deficiency research.

Partial deletion of short arm of a chromosome of the 4-5 group (Denver) in an adult male.

J. Delhanty, M. Ridler, J. M. Berg, 2008, Journal of mental deficiency research.

Long arm measurements of chromosomes 4 and 5 with special reference to the cri du chat syndrome

M. Ridler, J. Faunch, JANET A. FAUNCH, 1969, Annals of human genetics.

THE LONGITUDINAL STUDY OF THE LEUCOCYTE COUNT IN INFANTS WITH MONGOLISM

M. Ridler, A. Shapiro, 1959 .

An adult male with XYYY sex chromosomes

M. Ridler, P. Saldaña-Garcia, M. J. Mitchell, 1973, Clinical genetics.

Trisomy 16q arising from a maternal 15p;16q translocation.

M. Ridler, J. McKeown, 1979, Journal of medical genetics.

ON THE ASSOCIATION OF BROAD THUMBS AND FIRST TOES WITH OTHER PHYSICAL PECULIARITIES AND MENTAL RETARDATION

M. Ridler, G. F. Smith, B. W. Richards, 2008 .

Segregation of ABO, AK1 and ACONS in families with abnormalities of chromosome 9

J. E. Gray, C. Blank, M. Ridler, 1978, Annals of human genetics.

The incidence of Klinefelter's syndrome in a mental deficiency hospital.

M. Ridler, A. Shapiro, 2008, Journal of mental deficiency research.

Prenatal detection of monosomy 18p and trisomy 18q mosaicism with unexpected fetal phenotype.

M. Ridler, S. Sutton, 1986, Journal of medical genetics.

Familial occurrence of a small, supernumerary metacentric chromosome in phenotypically normal women.

M. Ridler, J. Timothy, J. M. Berg, 1970, Journal of medical genetics.

Sex Chromatin Survey of Women in a Special Psychiatric Hospital

M. Ridler, A. Mcquaid, J. M. Berg, 1969, Nature.

11q Aneuploidy: Partial monosomy and trisomy in the children of a mother with a t(3;11)(p27;q23) translocation

M. Ridler, J. McKeown, 1979, Human Genetics.

Banding patterns of metaphase chromosomes in Down's syndrome.

M. Ridler, 1971, Lancet.

Recurrent abortion associated with a balanced 22;22 translocation, or isochromosome 22q in a monozygous twin

M. Ridler, B. Lewis, 1977, Human Genetics.

Prenatal diagnosis and outcome of pregnancy in 2036 women investigated by amniocentesis

J. Squire, M. Ridler, S. Sutton, 1982, Human Genetics.

POSSIBLE SOURCE OF ERROR IN PRENATAL DIAGNOSIS VIA CHORIONIC VILLUS BIOPSY

M. Ridler, M. Grewal, 1984, The Lancet.

De Lange Syndrome: Report of a Case with an Unusual Karyotype

M. Ridler, G. F. Smith, B. Mccreary, 1967 .

Dermal patterns on the fingers and toes in mongolism.

M. Ridler, G. F. Smith, M. Bat-Miriam, 2008, Journal of mental deficiency research.

A Mosaic Mongol with Normal Leucocyte Chromosomes

J. Delhanty, M. Ridler, A. Shapiro, 1965, British Journal of Psychiatry.

Partial monosomy 7withinterstitial deletions intwo infants withdiffering congenital abnormalities

M. Ridler, M. Liberman, I. Kessel, 1979 .

Ultrastructure of banded human metaphase chromosomes.

M. Ridler, P. Ohara, 1972, Lancet.

Further examples of trisomy‐20 mosaicism in amniotic cell cultures

J. Barber, M. Ridler, M. S. Grewal, 1985, Prenatal Diagnosis.

A CASE OF PRADER‐WILLI SYNDROME IN A GIRL WITH A SMALL EXTRA CHROMOSOME

M. Ridler, O. Garrod, J. M. Berg, 1971, Acta paediatrica Scandinavica.

Association of D-D translocation with mongolism.

M. Ridler, J. M. Berg, J. Faunch, 2008, Journal of mental deficiency research.

Epiloia (tuberous sclerosis): a report of a case with unusual tumours.

M. Ridler, E. A. Green, J. M. Berg, 1966, Journal of Medical Genetics.