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51

Neural tube defects as an X-linked condition

Dr. Michael Baraitser, John Burn, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1984

Language:

english

File:

PDF, 130 KB

english, 1984

52

An autosomal recessive mental retardation syndrome with hepatic fibrosis and renal cysts

Dr. Elizabeth Thompson, Michael Baraitser, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 583 KB

english, 1986

53

Research into the origin and treatment of muscular dystrophy. Proceedings of a workshop held at „De Hooge Vuursche”, Baarn, Holland. L.P. ten Kate, P.L. Pearson, and A.M. Stadhouders, editors. Current Clinical Practice Series 20. Excerpta Medica: Amsterdam, 1984

Michael Baraitser, Ian H. Porter

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 77 KB

english, 1986

54

A new X-linked mental retardation syndrome

Robin Dawn Clark, Michael Baraitser, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 179 KB

english, 1987

55

DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): Elevated plasma and urinary 2-oxoglutarate in three unrelated patients

Dr. M. A. Patton, S. Krywawych, R. M. Winter, D. P. Brenton, M. Baraitser, Giovanni Neri

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 631 KB

english, 1987

56

Proteus syndrome: An expanded phenotype

Dr. Robin Dawn Clark, Dian Donnai, John Rogers, Jane Cooper, Michael Baraitser, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 3.44 MB

english, 1987

57

Nosology of Smith-Lemli-Opitz syndrome

Elizabeth Thompson, Michael Baraitser, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 80 KB

english, 1987

58

A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: Similarities to a report of aldolase a deficiency

J. A. Hurst, Dr. M. Baraitser, R. M. Winter, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 331 KB

english, 1987

59

Distinctive syndrome of short stature, craniosynostosis, skeletal changes, and malformed ears

J. A. Hurst, R. M. Winter, Dr. M. Baraitser, John M. Optiz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 492 KB

english, 1988

60

Midline facial defects with ocular colobomata

I. K. Temple, H. Brunner, B. Jones, J. Burn, M. Baraitser

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 517 KB

english, 1990

61

Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotype

Lyn S. Chitty, Rory McCrimmon, I. Karen Temple, Isobel M. Russell-Eggitt, Dr. Michael Baraitser

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 398 KB

english, 1991

62

Autosomal dominant transmission of congenital erythroid hypoplastic anemia with radial abnormalities

Dr. J. A. Hurst, M. Baraitser, B. Wonke

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 292 KB

english, 1991

63

Genetic and clinical heterogeneity of Stickler syndrome

Gillian M. Vintiner, I. Karen Temple, Helen R. Middleton-Price, Michael Baraitser, Dr. Sue Malcolm

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 494 KB

english, 1991

64

Severe mental retardation and absent nails of Hallux and Pollex

I. Karen Temple, Dr. Michael Baraitser

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 233 KB

english, 1991

65

Joubert syndrome: A review

Jorge M. Saraiva, Dr. Michael Baraitser

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 760 KB

english, 1992

66

Joubert syndrome with retinal dystrophy and renal cysts: Reply to Dr. Di Rocco

Michael Baraitser

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 53 KB

english, 1993

67

Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease

Dr. W. Reardon, A. Hockey, P. Silberstein, B. Kendall, T. I. Farag, M. Swash, R. Stevenson, M. Baraitser

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 1.39 MB

english, 1994

68

New case of the Carey-Fineman-Ziter syndrome

M. Baraitser, Dr. W. Reardon

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 171 KB

english, 1994

69

Male pseudohermaphroditism in sibs with the α-thalassemia/mental retardation (ATR-X) syndrome

Dr. W. Reardon, R. J. Gibbons, R. M. Winter, M. Baraitser

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 336 KB

english, 1995

70

Nonspecific X-linked mental retardation with macrocephaly and obesity: A further family

M. Baraitser, Dr. W. Reardon, S. Vijeratnam

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 361 KB

english, 1995

71

Regarding the ongoing discussion about the reporting of single cases

Michael Baraitser

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 57 KB

english, 2007

72

Genetic prediction in Huntington's disease: What are the limitations imposed by pedigree structure

V. Peter Misra, Michael Baraitser, Dr. A. E. Harding

Journal:

Movement Disorders

Year:

1988

Language:

english

File:

PDF, 242 KB

english, 1988

73

Effect of genetic counselling on the prevalence of huntington's chorea

C.O. Carter, K.A. Evans, M. Baraitser

Journal:

Patient Education and Counseling

Year:

1983

Language:

english

File:

PDF, 124 KB

english, 1983

74

Prenatal treatment of fetal hydrops associated with the hypertelorism-dysphagia syndrome (opitz-g syndrome)

M. A. Patton, M. Baraitser, K. Nickolaides, C. H. Rodeck, H. Gamsu

Journal:

Prenatal Diagnosis

Year:

1986

Language:

english

File:

PDF, 514 KB

english, 1986

75

Perlman and Wiedemann-Beckwith syndromes: Two distinct conditions associated with Wilms' tumour

R. G. Grundy, J. Pritchard, M. Baraitser, A. Risdon, M. Robards

Journal:

European Journal of Pediatrics

Year:

1992

Language:

english

File:

PDF, 735 KB

english, 1992

76

Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: A cautionary tale

John Burn, Michael Baraitser, David T. Hughes, Pedro Saldana-Garcia, James F. N. Taylor

Journal:

Pediatric Cardiology

Year:

1984

Language:

english

File:

PDF, 887 KB

english, 1984

77

The person behind the syndrome: Peter Beighton and Greta Beighton Springer-Verlag (231 pages), ISBN 3-540-76044-X, US $ 59.00, Hardback

Michael Baraitser

Journal:

Year:

1999

Language:

english

File:

PDF, 13 KB

english, 1999

78

Look who’s taking notes in your clinic: mystery shoppers as evaluators in sexual health services

Paula Baraitser, Vikki Pearce, Nathalie Walsh, Richard Cooper, Kirsty Collander Brown, Jo Holmes, Lovelle Smith, Petra Boynton

Journal:

Health Expectations

Year:

2008

Language:

english

File:

PDF, 116 KB

english, 2008

79

GROUPWORK WITH MOTHERS WHO HAVE BEEN SEXUALLY ABUSED IN CHILDHOOD

Amélie Noack, Lisa Baraitser

Journal:

British Journal of Psychotherapy

Year:

2004

Language:

english

File:

PDF, 78 KB

english, 2004

80

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes

Rutland, Paul, Pulleyn, Louise J., Reardon, William, Baraitser, Michael, Hayward, Richard, Jones, Barry, Malcolm, Sue, Winter, Robin M., Oldridge, Michael, Slaney, Sarah F.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 429 KB

1995

81

Turner syndrome: Edited by Ron G. Rosenfeld and Melvin M. Grumbach Marcel Dekker Inc., New York, 552 pp

Michael Baraitser

Journal:

Early Human Development

Year:

1990

Language:

english

File:

PDF, 39 KB

english, 1990

82

ORGANIC ACIDURIAS AND AMINO ACIDURIAS IN THE AETIOLOGY OF LONG-TERM MENTAL HANDICAP

R. W. E. WATTS, M. BARAITSER, R. A. CHALMERS, P. PURKISS

Journal:

Journal of Intellectual Disability Research

Year:

1980

Language:

english

File:

PDF, 3.43 MB

english, 1980

83

NATURAL HISTORY, SYMPTOMS AND TREATMENT OF THE NARCOLEPTIC SYNDROME

J. D. Parkes, M. Baraitser, C. D. Marsden, P. Asselman

Journal:

Acta Neurologica Scandinavica

Year:

1975

Language:

english

File:

PDF, 838 KB

english, 1975

84

The Walker-Warburg or a new syndrome?

Dr. Michael Baraitser, Jonathan Dossetor, Sarah Slaney, Andrew Green

Journal:

Acta Ophthalmologica (Blackwell)

Year:

1996

Language:

english

File:

PDF, 358 KB

english, 1996

85

A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection

J. Burn, H. T. Wickramasinghe, B. Harding, M. Baraitser

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 337 KB

english, 1986

86

A family with congenital suprabulbar paresis (Worster-Drought syndrome)

M. A. Patton, M. Baraitser, E. M. Brett

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 252 KB

english, 1986

87

The Angelman (Happy Puppet) syndrome: is it autosomal recessive?

M. Baraitser, M. Patton, S. T. S. Lam, E. M. Brett, J. Wilson

Journal:

Clinical Genetics

Year:

1987

Language:

english

File:

PDF, 1.86 MB

english, 1987

88

Hereditary neurocutaneous angiomatous malformations: autosomal dominant inheritance in two families

Jane Hurst, Michael Baraitser

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 503 KB

english, 1988

89

Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?

William Reardon, I. Karen Temple, Barry Jones, Michael Baraitser

Journal:

Clinical Genetics

Year:

1990

Language:

english

File:

PDF, 311 KB

english, 1990

90

Partial lipodystrophy syndromes – a further male case

W. Reardon, I. K. Temple, H. Mackinnon, J. V. Leonard, M. Baraitser

Journal:

Clinical Genetics

Year:

1990

Language:

english

File:

PDF, 448 KB

english, 1990

91

Atypical facio-scapulo-humeral muscular dystrophy — a counselling dilemma

W. Reardon, I. K. Temple, G. Harwood, M. Baraitser

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 569 KB

english, 1991

92

Reply

Michael Baraitser

Journal:

Clinical Genetics

Year:

1995

Language:

english

File:

PDF, 77 KB

english, 1995

93

Severe Microcephaly Associated with Congenital Varicella Infection

I. E. Scheffer, M. Baraitser, E. M. Brett

Journal:

Developmental Medicine & Child Neurology

Year:

1991

Language:

english

File:

PDF, 620 KB

english, 1991

94

The FG syndrome: 7 new cases

E. M. Thompson, M. Baraitser, R. H. Lindenbaum, Z. H. Zaid, J. S. Kroll

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 1.11 MB

english, 1985

95

Axonal velocities of motor units in the hand and foot muscles of the baboon

R.W. Gilliatt, H.C. Hopf, P. Rudge, M. Baraitser

Journal:

Journal of the Neurological Sciences

Year:

1976

Language:

english

File:

PDF, 569 KB

english, 1976

96

Primidone teratogenicity or noonan syndrome?

John Burn, Michael Baraitser

Journal:

The Journal of Pediatrics

Year:

1982

Language:

english

File:

PDF, 82 KB

english, 1982

97

A distinctive type of hypohidrotic ectodermal dysplasia featuring hypothyroidism

Michael G. Pike, Michael Baraitser, Robert Dinwiddie, David J. Atherton

Journal:

The Journal of Pediatrics

Year:

1986

Language:

english

File:

PDF, 1.39 MB

english, 1986

98

Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case

RobinM. Winter, DallasM. Swallow, Michael Baraitser, Paul Purkiss

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 694 KB

english, 1980

99

Intrafamilial correlation in Friedreich's ataxia

R. M. Winter, A. E. Harding, M. Baraitser, M. B. Bravery

Journal:

Clinical Genetics

Year:

1981

Language:

english

File:

PDF, 483 KB

english, 1981

100

Heterogeneity and pleiotropism in the Moebius syndrome Sirs

Michael Baraitser

Journal:

Clinical Genetics

Year:

1982

Language:

english

File:

PDF, 100 KB

english, 1982