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Transient neonatal tyrosinaemia

Journal of inherited metabolic disease, 1989-03, Vol.12 (1), p.13-22

1989

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Clinical and Genetic Problems in Familial Intestinal Polyposis

Gut, 1960-12, Vol.1 (4), p.285-290

Veale, A. M. O.

1960

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Possible Autosomal Linkage in Man

Nature (London), 1958-08, Vol.182 (4632), p.409-410

VEALE, A. M. O

1958

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Inheritance of hypertrophic cardiomyopathy: a cross sectional and M mode echocardiographic study of 50 families

British Heart Journal, 1987-09, Vol.58 (3), p.259-266

1987

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Segregation Analysis of A Large t(21q22q) Family

Journal of medical genetics, 1973-12, Vol.10 (4), p.362-366

1973

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ポリネシア、エリス島人の指紋

人類學雜誌, 1968, Vol.76(5), pp.205-214

1968

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ニュージランドマオリの指紋

人類學雜誌, 1965/07/30, Vol.73(2), pp.33-49

1965

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Polynesian Finger Prints: Ellice Islanders

Journal of the Anthropological Society of Nippon, 1968, Vol.76(5), pp.205-214

1968

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Finger-Prints of the New Zealand Maori

Journal of the Anthropological Society of Nippon, 1965/07/30, Vol.73(2), pp.33-49

1965

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B. HALLGREN and T. SJOGREN. "A Clinical and Genetico-statistical Study of Schizophrenia and Low-grade Mental Deficiency in a Large Swedish Rural Population" (Book Review)

Population Studies, 1960, Vol.14 (1), p.170

Veale, A M O

1960

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T. LARSSON and T. SJOGREN. "Essential Tremor" (Book Review)

Population Studies, 1960, Vol.14 (1), p.171

Veale, A M O

1960

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B. HALLGREN. "Retinitis Pigmentosa Combined with Congenital Deafness: With Vestibulo-Cerebellar Ataxia and Mental Abnormality in a Proportion of Cases" (Book Review)

Population Studies, 1960, Vol.14 (1), p.170

Veale, A M O

1960

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Leukemia in Close Relatives—Accident or Predisposition?

JNCI : Journal of the National Cancer Institute, 1969-03, Vol.42 (3), p.517-524

1969

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Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndrome

Clinical genetics, 1979-09, Vol.16 (3), p.151-155

1979

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Integration of human genetic studies in clinical medicine

Journal of the Royal College of Physicians of London, 1971-10, Vol.6 (1), p.41

Veale, A M

1971

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Are 1q+ chromosomes harmless?

Clinical genetics, 1974-11, Vol.6 (5), p.383-393

1974

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De novo translocation Down's syndrome: Risk of recurrence of Down's syndrome

Clinical genetics, 1974-01, Vol.6 (3), p.160-164

1974

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The formation of the abnormal chromosome in balanced homologous Robertsonian translocation carriers

Human genetics, 1974-01, Vol.21 (3), p.279-282

1974

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Giemsa banding in the t(13q13q) carrier mother of a translocation trisomy 13 abortus

Human genetics, 1973-04, Vol.18 (2), p.183-184

1973

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XXXX syndrome: case report, and a note on genetic counselling and fertility

Humangenetik, 1973-01, Vol.17 (4), p.323-330

1973

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A girl with severe expression of the Holt-Oram gene

Clinical genetics, 1973-01, Vol.4 (5), p.417-421

1973

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Introduction to Quantitative Genetics

Applied Statistics, 1960, Vol.9 (3), p.202-203

Veale, A. M. O.

1960

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Retinitis Pigmentosa Combined with Congenital Deafness: with Vestibulo- Cerebellar Ataxia and Mental Abnormality in a Proportion of Cases

Population Studies, 1960, Vol.14 (2), p.170-170

Veale, A. M. O.

1960

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A Metabolic Survey of the Mentally Retarded of Fiji

The Australian journal of mental retardation, 1976, Vol.4 (2), p.33-37

1976

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Basal and supplemental blood pressures in relationship to life expectancy and hypertension symptomatology

New Zealand medical journal, 1959-12, Vol.58, p.711

1959

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Transient neonatal tyrosinaemia

Clinical and Genetic Problems in Familial Intestinal Polyposis

Possible Autosomal Linkage in Man

Inheritance of hypertrophic cardiomyopathy: a cross sectional and M mode echocardiographic study of 50 families

Segregation Analysis of A Large t(21q22q) Family

ポリネシア、エリス島人の指紋

ニュージランドマオリの指紋

Polynesian Finger Prints: Ellice Islanders

Finger-Prints of the New Zealand Maori

B. HALLGREN and T. SJOGREN. "A Clinical and Genetico-statistical Study of Schizophrenia and Low-grade Mental Deficiency in a Large Swedish Rural Population" (Book Review)

T. LARSSON and T. SJOGREN. "Essential Tremor" (Book Review)

B. HALLGREN. "Retinitis Pigmentosa Combined with Congenital Deafness: With Vestibulo-Cerebellar Ataxia and Mental Abnormality in a Proportion of Cases" (Book Review)

Leukemia in Close Relatives—Accident or Predisposition?

Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndrome

Integration of human genetic studies in clinical medicine

Are 1q+ chromosomes harmless?

De novo translocation Down's syndrome: Risk of recurrence of Down's syndrome

The formation of the abnormal chromosome in balanced homologous Robertsonian translocation carriers

Giemsa banding in the t(13q13q) carrier mother of a translocation trisomy 13 abortus

XXXX syndrome: case report, and a note on genetic counselling and fertility

A girl with severe expression of the Holt-Oram gene

Introduction to Quantitative Genetics

Retinitis Pigmentosa Combined with Congenital Deafness: with Vestibulo- Cerebellar Ataxia and Mental Abnormality in a Proportion of Cases

A Metabolic Survey of the Mentally Retarded of Fiji

Basal and supplemental blood pressures in relationship to life expectancy and hypertension symptomatology

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