Volume 18; Issue 3

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Clinical Genetics
Volume 18; Issue 3

Clinical Genetics

Volume 18; Issue 3

1

Guadalajara camptodactyly syndrome : A distinct probably autosomal recessive disorder

J. M. Cantú, H. Rivera, Z. Nazará, Q. Rojas, A. Hernández, D. García-Cruz

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 591 KB

english, 1980

2

Genetic susceptibility to multiple sclerosis: a linkage analysis with age-of-onset corrections

R. W. Haile, S. E. Hodge, B. R. Visscher, M. A. Spence, R. Detels, T. L. McAuliffe, M. S. Park, J. P. Dudley

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 539 KB

english, 1980

3

Genetic counselling for adult polycystic kidney disease. Ultrasound a useful tool in pre-symptomatic diagnosis?

BarendL. Hogewind, JanJ. Veltkamp, CornelisW. Koch, Jaap de Graeff

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 301 KB

english, 1980

4

Familial Williams Syndrome

X. Cortada, K. Taysi, A. F. Hartmann

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 310 KB

english, 1980

5

Pitfalls in the prenatal diagnosis of propionic acidemia

P. D. Buchanan, S. G. Kahler, L. Sweetman, W. L. Nyhan

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 448 KB

english, 1980

6

Addison disease and cerebral sclerosis in an apparently heterozygous girl: evidence for inactivation of the adrenoleukodystrophy locus

W. Heffungs, H. Hameister, H. H. Ropers

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 357 KB

english, 1980

7

Chlorpropamide-alcohol flushing is not useful for individual genetic counseling of diabetic patients

M. Dreyer, J. Kühnau, H. W. Rüdiger

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 123 KB

english, 1980

8

Familial occurrence of intracranial arterial occlusive disease (Moyamoya) in neurofibromatosis

RobertP. ERICKSON, James Woolliscroft, RichardJ. Allen

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 555 KB

english, 1980

9

HLA typing of cultured amniotic cells for the prenatal diagnosis of complement C4 deficiency

MarilynS. Pollack, HansD. Ochs, Bo Dupont

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 262 KB

english, 1980

10

Prior abortions and neural tube defects

T. J. David, P. A. Townley, AmandaR. Goldstein

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 133 KB

english, 1980

11

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

12

Dominantly inherited macular degeneration (Best's disease) in a homozygous father with 11 children

S. Nordström, W. Thorburn

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 342 KB

english, 1980

13

Prenatal detection of intestinal obstruction: deficient amniotic fluid disaccharidases in affected fetuses

P. R. Morin, M. Potier, L. Dallaire, S. B. Melançon, A. Milunsky

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 316 KB

english, 1980

14

Abnormalities of sexual differentiation in campomelic dwarfs

R. M. Pauli, R. A. Pagon

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 242 KB

english, 1980

15

A modified method for the identification of heterozygotes for Gaucher's disease using differential thermal inactivation

Charles Goodman, JohnS. O'Brien

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 312 KB

english, 1980

16

Announcements

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 54 KB

english, 1980