Volume 22; Issue 5

Journal of Medical Genetics

Volume 22; Issue 5

1

Sacrococcygeal teratoma and normal alphafetoprotein concentration in amniotic fluid.

Szabo, M, Varga, P, Zalatnai, A, Hidvegi, J, Toth, Z, Papp, Z

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 816 KB

english, 1985

2

Familial absence of the pectoralis major, serratus anterior, and latissimus dorsi muscles.

David, T J, Winter, R M

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 499 KB

english, 1985

3

Osmotic fragility test in heterozygotes for alpha and beta thalassaemia.

Maccioni, L, Cao, A

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 360 KB

english, 1985

4

Stanley Walker, BSc, PhD

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 233 KB

english, 1985

5

A family study of hidradenitis suppurativa.

Fitzsimmons, J S, Guilbert, P R

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 771 KB

english, 1985

6

Classroom teaching in genetics and birth defects: the Nottingham experience.

Fitzsimmons, J S

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 693 KB

english, 1985

7

Attitudes of Asian families to genetic counselling.

Mehta, L, Young, I D

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 172 KB

english, 1985

8

Reciprocal translocation between chromosomes 8 and 9 in atypical chronic myeloid leukaemia.

Oscier, D G, Mufti, G J, Gardiner, A, Hamblin, T J

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 719 KB

english, 1985

9

Parietal foramina in the Saethre-Chotzen syndrome.

Young, I D, Swift, P G

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 479 KB

english, 1985

10

The Nager acrofacial dysostosis syndrome with the tetralogy of Fallot.

Thompson, E, Cadbury, R, Baraitser, M

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 652 KB

english, 1985

11

Genetics and biochemical variability of variants of 21 hydroxylase deficiency.

Gordon, M T, Conway, D I, Anderson, D C, Harris, R

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 831 KB

english, 1985

12

Periconceptional vitamin supplementation and the prevention of neural tube defects.

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 353 KB

english, 1985

13

Partial 2p deletion in a girl with a complex chromosome rearrangement involving chromosomes 2, 6, 11, and 21.

Young, R S, Medrano, M A, Hansen, K L

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 948 KB

english, 1985

14

The human Y chromosome.

Goodfellow, P, Darling, S, Wolfe, J

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 2.73 MB

english, 1985

15

The first observation of Hb D Punjab beta zero thalassaemia in an English family with 22 cases of unsuspected beta zero thalassaemia minor among its members.

Worthington, S, Lehmann, H

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 543 KB

english, 1985

16

Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype.

Patton, M A, Laurence, K M

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 861 KB

english, 1985

17

Philtrum length, intercommissural distance, and ear measurements in newborn infants.

Sivan, Y, Merlob, P, Reisner, S H

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 417 KB

english, 1985

18

Chronic proximal spinal muscular atrophy of childhood and adolescence: problems of classification and genetic counselling.

Hausmanowa-Petrusewicz, I, Zaremba, J, Borkowska, J

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 523 KB

english, 1985

19

The genetic control of phenformin 4-hydroxylation.

Shah, R R, Evans, D A, Oates, N S, Idle, J R, Smith, R L

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 719 KB

english, 1985

20

Correspondence

Seller, M J, Nevin, N C

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 351 KB

english, 1985

21

Phenotypic variation in LADD syndrome.

Thompson, E, Pembrey, M, Graham, J M

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 678 KB

english, 1985

22

Correction

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 95 KB

english, 1985

23

Abstracts of the meeting of the Clinical Genetics Society. 24-25 April 1985, Birmingham.

Journal:

Journal of Medical Genetics

Year:

1985

Language:

english

File:

PDF, 793 KB

english, 1985