Bibliography of Human Genetics

Overview

Journal Am J Hum Genet

Publisher Cell Press

Specialty Genetics

Date 1958 Dec 1

PMID 13606121

Authors

R H Post

Affiliations

Soon will be listed here.

References

ANDERSON E, KALCKAR H, Isselbacher K . A specific enzymatic defect in congenital galactosemia. Acta Genet Stat Med. 1957; 7(1):187-8. DOI: 10.1159/000150961. View

MacDonald A, Shanks R . Hypophosphatasia. Arch Dis Child. 1957; 32(164):304-10. PMC: 2012130. DOI: 10.1136/adc.32.164.304. View

ANDERSON Jr A, EMMEL G . Diffuse interstitial pulmonary fibrosis: the Hamman-Rich Syndrome. J Fla Med Assoc (1914). 1958; 44(7):702-9. View

Bull C . Metastatic choroiditis occurring in the course of pneumonia due to grippe, based on a study of six cases with two autopsies. Trans Am Ophthalmol Soc. 2014; 9:316-28. PMC: 1322460. View

Hauge M, HARVALD B . Genetics in intracranial tumours. Acta Genet Stat Med. 1957; 7(3):573-91. View

EDMUND J . Blepharophimosis congenita. Acta Genet Stat Med. 1957; 7(2):279-84. DOI: 10.1159/000150985. View

KHERUMIAN R, Durand M, METIANU C, MOULLEC J, KHERUMIAN-ALLARY O . [Genetic etiology of congenital heart diseases]. Acta Genet Stat Med. 1957; 7(1):213-4. View

Bulmer M . The numbers of human multiple births. Ann Hum Genet. 1958; 22(2):158-64. DOI: 10.1111/j.1469-1809.1957.tb01931.x. View

Crocker A, Farber S . Niemann-Pick disease: a review of eighteen patients. Medicine (Baltimore). 1958; 37(1):1-95. DOI: 10.1097/00005792-195802000-00001. View

10.

McCULLAGH E, LEISER A . Turner's syndrome and Laurence-Moon-Biedl syndrome in siblings. J Clin Endocrinol Metab. 1957; 17(8):985-8. DOI: 10.1210/jcem-17-8-985. View

11.

HORDER M . [Congenital familial deficiency of factor VII with additional defect of thromboplastin formation]. Acta Haematol. 1958; 19(1):30-9. DOI: 10.1159/000205411. View

12.

Zampi G, CINTI G . [Congenital goiter in twins]. Arch De Vecchi Anat Patol. 1957; 27(2):443-69. View

13.

DE BLECOURT-MEINDERSMA T . Hereditary factors in some rheumatic diseases. Acta Genet Stat Med. 1957; 7(1):144-7. View

14.

BECKER P . [New results of genetics of muscular dystrophy]. Acta Genet Stat Med. 1957; 7(2):303-10. View

15.

Van Zonneveld R, POLMAN A . Hereditary factors in longevity. Acta Genet Stat Med. 1957; 7(1):160-2. DOI: 10.1159/000150955. View

16.

JUEL E, Vogt E . The frequency of the Duffy blood group antigens in 1000 Oslo blood donors as defined by anti-Fya. Acta Pathol Microbiol Scand. 1958; 42(2):150-2. DOI: 10.1111/j.1699-0463.1958.tb03179.x. View

17.

CHERNOFF A . The hemoglobin D syndromes. Blood. 1958; 13(2):116-27. View

18.

Esteve R . Idiopathic scoliosis in identical twins. J Bone Joint Surg Br. 1958; 40-B(1):97-9. DOI: 10.1302/0301-620X.40B1.97. View

19.

Forni S . [New genealogical tree of degeneration typeto-retinal of the macular and peripapillary region, type "malattia leventinese"]. Bibl Ophthalmol. 1957; 12(47):570-5. View

20.

VERDURA G . [Auxological data on twin premature infants]. Minerva Pediatr. 1957; 9(51-52):1636-8. View