Acta geneticae medicae et gemellologiae: twin research: Volume 1 -

Acta geneticae medicae et gemellologiae: twin research

Only show content I have access to (83)

Over 3 years (83)

View selected items
Save to my bookmarks
Export citations
Download PDF (zip)
Save to Kindle
Save to Dropbox
Save to Google Drive
Save content to
To save this undefined to your undefined account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you used this feature, you will be asked to authorise Cambridge Core to connect with your undefined account. Find out more about saving content to .

To save this article to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Please be advised that item(s) you selected are not available.
You are about to save
Acta geneticae medicae et gemellologiae: twin research
ISSN: 0001-5660

EISSN: 2059-6324

URL: /core/journals/amg-acta-geneticae-medicae-et-gemellologiae-twin-research
Your Kindle email address

Please provide your Kindle email.

@free.kindle.com @kindle.com (service fees apply)

By using this service, you agree that you will only keep content for personal use, and will not openly distribute them via Dropbox, Google Drive or other file sharing services

Acta geneticae medicae et gemellologiae: twin research

Refine listing

Actions for selected content:

Volume 1 - January 1952

Recensioni

T. Kemp. Arvehygiejne. Ejnar Munksgaard, Kobenhavn 1951.

Jan Mohr. Vitiligo in a pair of monovular Twins. Acta Genet, et Stat. Med. 2, 3. 1951.

W. Dölle. Bine weitere Ergänzung des Weilschen Diabetes - insipidus Stammbaumes. Ztschr. menschl. Vererb. u. Konstitutionslehre. 30, 3. 1951.

A. Giordano. Enzimopenie ereditarie. Folia Hered. Path. vol. I, fasc. I (Luglio 1951).

M. Lamy, C. Launay, M. Soulé. Dyslexie spécifique chez jumeaux identiques. La Semaine des Hopitaux. 28e année, n. 35 (1952).

N. Rossi. La poliposi ereditaria del crasso. Folia Hered. Path. vol. I, fasc. I. (Luglio 1951)

William G. Lennox. The heredity of epilepsy as told by relatives and twins. J.A.M.A. 146, pp. 529–536, giugno 1951.

C. J. Reitz. Rudimentêre occipitale arm. South African Medical Journal. Vol. 26, n. 15 (1952).

Walter Brenner. Zur Frage der Erblichkeit von Microcephalic und Hydrocephalie. Ztschr. menschl. Vererb. u. Konstitutionslehre. 30, 3. 375. 1951.

E. J. Gardner and H. P. Plenk. Hereditary Pattern for Multiple Osteomas in a Family Group. Am. J. Human Genet. Vol. 4, n. 1 (1952).

M. Zorzi. Le malformazioni diverticolari giganti del grosso intestino come fenomeno di gemellarità circoscritta. Folia Hered. Path. vol. I, fasc. I (Luglio 1951).

A. S. Wiener. Heredity of the M-N-S Blood Types. Theoretico-Statistical Considerations. Am. J. Human Genet. Vol. 4, n. 1 (1952).

I. Moretti. Confronto tra eritroolastosi fetale e sifilide congenita e loro comportamento nei gemelli. Folia Hered. Path, vol. I, fasc. II, (Ottobre 1951).

John W. Schut. Hereditary ataxia. Am. J. Human. Genetic. 3, 2, 93. 1951.

Charles Richet, Maurice Rymer et Jacqyes Besse. nanisme et infantilisme hypophysaires chez une hexadactyle héréditaire. La Semaine des Hopitaux, 27e Année, n. 53–54, 18–22 juillet 1951.

G. Pintus. Mutazione e somazione. Folia Hered. Path. vol. I fasc. II (Ottobre 1951).

L. Gedda. Psicologia e Linguaggio. Prolusione all’Anno Accademico 1951-1952. Istituto Universitario Maria SS. Assunta. Roma.

v. Verschuer, Otmar Frhr. Humangenetik körperliche Erbkranicheiten). Münch. med. Wschr. 49–51 (1951).

M. Ebnother. Ueber eme familiäre Skelettstörung mit multiloculären, aseptischen Knochennekrosen, insbesondere mit Osteochondrosis dissecans. Inaugural-Dissertation. Universität Zürich, 1952.

P. Brisotto. A proposito di un cancro del mesofaringe. Oto-rino-laringologia Italiana, vol. XIX, fasc. III. 1951.

Acta geneticae medicae et gemellologiae: twin research

Refine listing

Actions for selected content:

Save Search

Volume 1 - January 1952

Recensioni