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Volume 14; Issue 1
Main
Clinical Genetics
Volume 14; Issue 1
Clinical Genetics
Volume 14; Issue 1
1
Presymptomatic diagnosis of adult onset polycystic kidney disease by ultrasonography
B. Wolf
,
A. T. Rosenfield
,
K. J. W. Taylor
,
N. Rosenfield
,
S. Gottlieb
,
Y. E. Hsia
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 467 KB
Your tags:
english, 1978
2
Apparently non-deleted ring-1 chromosome and extreme growth failure in a mentally retarded girl
B. Kjessler
,
K.-H. Gustavson
,
A. Wigertz
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 533 KB
Your tags:
english, 1978
3
Atypical expression of ß-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalities
Generoso Andria
,
Ennio Del Giudice
,
Arnold J. J. Reuser
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 578 KB
Your tags:
english, 1978
4
The Dyggve – Melchior – Clausen syndrome in adult siblings
R. P. Bonafede
,
P. Beighton
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 482 KB
Your tags:
english, 1978
5
H - Y antigen in human intersexuality
S. N. Ghosh
,
P. N. Shah
,
H. M. Gharpure
,
Usha Athreya
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 293 KB
Your tags:
english, 1978
6
In vitro studies of the interaction of isolated Lp(a) lipoprotein and other serum lipoproteins with glycosaminoglycans
G. Dahlén
,
C. Ericson
,
K. Berg
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 413 KB
Your tags:
english, 1978
7
Charcot-Marie-Tooth disease: Data for genetic counseling relating age to risk
Thomas D. Bird
,
George H. Kraft
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 482 KB
Your tags:
english, 1978
8
Biochemical investigations in cultured skin fibroblasts from patients with Duchenne muscular dystrophy
S. D. J. Pena
,
A. Vust
,
D. Tucker
,
J. L. Hamerton
,
K. Wrogemann
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 280 KB
Your tags:
english, 1978
9
The cherry red spot—myoclonus syndrome: A newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiency
John S. O'Brien
Journal:
Clinical Genetics
Year:
1978
Language:
english
File:
PDF, 383 KB
Your tags:
english, 1978
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