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BIBLIOGRAPHY OF HUMAN GENETICS

THIS section, prepared by the Editor, continues the current list of research articles and books of
interest to students of human heredity. For information concerning the arrangement of titles, abbreviations for medical serials, and authors' addresses, see Part I of the 1949 list (Am. J. Human
Genet. 1:105-112). Numbers placed in square brackets following citations in the present list ([1],
[2], [31, [4]) refer to earlier parts of the 1949 list, where the author's address is provided.

1950-PART 2
ANDRESEN, P. H., ANDERSEN, A., JORDAL, K., & HENNINGSEN, K. Correlation entre le
systeme Lewis et le systeme sekreteur-non-secreteur; recherches sur 71 familles. Rev.
hemat. 5(3-4): 305-314. [3]
BAGGI, G., FIORENTINI, S., & RoMEi, L. Alterazioni stomatologiche in giovinetta rivelatrici
di emopatia presente allo stato latente e conclamato nei familiari. Riv. ital. stomat.

5(6): 621-630.
BALDI, E. M., MARGULIES, M., & BAYONA, E. Consideraciones sobre un caso de un niflo
Rh0-negativo en un matrimonio con isoimmunizaci6n maternofetal. Obst. gin. latino
am. 8(3-4): 119-121.
BARNICOT, N. A. Taste deficiency for phenylthiourea in African negroes and Chinese. Ann.
Eugen., Cambr. 15(3): 248-254.
BENACH CARRERAS, B. La importancia de la reaccion anamnestica en la conflicto fetomaterno. Vida nueva, Habana, 65(5): 164-166.
BERITIC, T. Cyanosis methaemoglobinaemica hereditaria. Lijec vjes. 72(4-5): 162-166.
BERTINSHAW, D., LAWLER, S. D., et al. The combination of blood groups in a sample of 475
people in a London hospital. Ann. Eugen., Cambr. 15(3): 234-242. [Lister Inst., London S.W.1, Eng.]
BOYD, W. C. Genetics and the Races of Man. Boston: Little, Brown & Co. Pp. 453, with 52
text figures. [1]
BoYD, W. C. Taste reactions to antithyroid substances. Science, 112(2901): 153.
BoYD, W. C. Use of blood groups in human classification. Science, 112(2903): 187-196.
BRYCE, L. M., JAKOBOWICZ, R., et al. Blood-group frequencies in a mother and infant sample
of the Australian population. Ann. Eugen., Cambr. 15(3): 271-275. [Jackobowicz: 4]
Bussi, L. Ulteriore contributo allo studio della genesi delle anomalie eritrocitiche nella
sindrome di Rietti-Greppi-Micheli. Policlinico. Sez. med. 57(3): 164-172.
CARCASSI, U., BINAGHI, G., ARGIOLAS, N., & LURIDIANA, S. Ricerche sul favismo. 1) Prime
osservazioni sul quadro ematologico familiare e su alcune alterazioni sierologiche in
pazienti di favismo. Rass. med. sarda, 52(3): 140-155.
CARDIS, F. Le probleme de l'heredite dans la tuberculose. Praxis, 39(34): 740-742.
CAZAL, P., & GRAAFLAND, R. Les groupes sanguins dans la population Montpellieraine;
repartition de l'antigene Rh; haute frequence des sujets Rh. Sang, 21(7): 623-627.
CUENDET, J. F., & DELLA PORTA, V. Association de nystagmus congenital, d'amblyopie
et d'astigmatisme corneen; heredite incompletement dominante liee au sexe. Arch.
opht., Par. 10(2): 187-201. [2]
CUMNS, H., TALLEY, C., & PLATOU, R. V. Palmar dermatoglyphics in mongolism. Pediatrics, S. Louis, 5(2): 241-248.
CUSMANO, L. Le embriopatie genotipiche. Minerva gin. 2(6): 246-248.
DE KROMME, L., & VAN DER SPEK, L. A. M. On placenta permeability and antibody varieties in Rhesus immunization. Mschr. kindergeneesk. 18(3-4): 130-145. [4]
409

BIBLIOGRAPHY, 1950, PART 2

410

DE LANGE, C. A not hitherto described variety of Krabbe's infantile form of diffuse hereditary brain-sclerosis. Fol. psychiat. &c. neerl. 53(2): 334-341.
DUBOIS-PREVOST, R. Parodontose et heredite. Paradentologie, 4(2): 62-67.
FALLS, H. F. Primary choroidoretinal aberrations with night blindness; genetics. Tr. Am.
Acad. Ophth. Otolar. July-Aug. 1950: 617-628. [1]
FANG, T. C. The third interdigital patterns on the palms of the general British population,
mongoloid and non-mongoloid, mental defectives. J. Ment. Sc., Lond. 96(404): 780787. [Dept. Zoology, Univ. Toronto, Ont. Can.]
FERRARIO, E. Sulla diagnosi radiologica di malformazione fetale e sull'azione dei raggi
roentgen sul prodotto del concepimento. Minerva gin. 2(6): 251-254.
FERRARIO, E., & FORTINA, A. Dati clinico-statistici sulle malformazioni fetali osservate nella
maternita e nel commune di Novara nell'ultimo ventennio. Minerva gin. 2(6): 248-251.
FEUERLICHT, N. Recurrent anencephaly. J. Am. M. Ass. 143(1): 23.
FONTAINE, J. Nephrose lipoidique, nephrite gravidique et facteur Rhesus. Bull. Ass. gyn.
obst. fr. 2(3): 301-302.
Par.
GALLOT, J. Heredite et maladies hereditaires en neuro-psychiatrie infantile. Vie
31(5): 16-21.
GEDDA, L. Lo studio dei gemelli nella scienza. Minerva med., Tor. 41(37): 213-216. [3]
GRUBB, R. Quelques aspects de la complexite des groupes ABO. Rev. htmat. 5(3-4): 268275. [2]
H. Animal genetics and orthodontics. Dent. Rec. 70(6): 152-160. [Dept.
Genetics, Univ. London, W.C.1, Eng.]
GUASCH, J. El factor Rh en Espafia. Rev. espant. pediat. 6(3): 387-390. [2]
GUTMAN, A. Ptosis congenital simple dans 5 generations. Acta genet. 1(4): 295-312. [Clinique
Ophtalmologique, Univ. Geneve, Switz.]
HENNINGSEN, K. etude d'ensemble du facteur sanguin P. Rev. hemat. 5(3-4): 276-284. [3]
HIRSZFELD, L. Les avortements la lumiere de l'immunologie et de la genetique. MMd. &
hyg. 8(176): 299. [Inst. de Microbiologie medicale, Univ. Warsaw, Poland]
ILG, F., & AMLES, L. B. Le point de vue genetique. Enfance, 3(2): 93-107.
JONSSON, A. B. Om Rh: s u-ndergruppsystem och dessvairde som bevismedel i faderskapsarenden. Social med. tskr. 27(6): 139-144; 27(7): 158-166.
JOSEF,C. Pfispevek k profylaxi fetalni erythroblastosy vtehotenstvi. [Prevention of fetal
erythroblastosis in pregnancy]. Cesk. gyn. 15(4-5): 353-364.
L. N. K kritike tak nazyvaemogo ucheniia o konstitutsii cheloveka. [Comment on
the so-called teaching about human constitution]. Ter. arkh. 22(3): 3-16.
KLEIN, D. De l'importance des recherches genetiques dans les maternites. Med. & hyg.
8(175,bis): 297-298. [Clinique Ophtalmologique, Univ. Geneve, Switz.]
LAWLER, S. D. The inheritance of the Lutheran blood groups in forty-seven English families.
Ann. Eugen., Cambr. 15(3): 255-257. [2].
LAWLER, S. D., BERTINSHAW, D., et al. Inheritance of the Rh blood groups: 150 families
tested withanti-C-c-C-D-E and anti-e. Ann. Eugen., Cambr. 15(3): 258-270.
LEJMBACH, Z. Dysporia entero-broncho-pancreatica congenita familiaris. Pediat. polska,
23(7-8): 723-734.
LELONG, M., & SOULIER, J. P. Sur une maladie hemorragique constitutionnelle characterisee par
l'allongement isole du temps de saignement (maladie de Willebrand:etude
de 9 cas). Rev.
himat. 5(1): 13-23. [2]
LUCIA, S. P., & HUNT, M. L. The significance of ABO compatibility and its relationship to
the intensity of Rh immunization. Blood, Balt. 5(8): 767-772. [2]
LUCIA, S. P., &HUNT, M. L. Hematologic features which may influence Rh immunization.
md.,

GRUJNEBERG,

K1ARLK,

California M. 73(3):

250-253.

BIBLIOGRAPHY, 1950, PART 2

411

MACGREGOR, A. G., & HARRISON, H. Congenital total colour blindness associated with
otosclerosis. Anun. Eugen., Cambr. 15(3): 219-233. [Dept. Pharmacology, Univ. Sheffield,
Eng.]
MATHER, K. Early days of genetics in Britain. Nature, Lond. 165(4208): 996-997. [1]
MATTEI, C., & LuCCI, M. Stati disfunzionali digestivi nelle sindromi microcitemiche. Riv.
crit. clin. med. 50(1): 5-52.
M0LGAARD, B. Om arvelighed af mavesar. [Heredity of peptic ulcer]. Ugeskr. laeger, 112(20):
707-709.
MORGANTI, G. Genetique generale et genetique des groupes sanguins ABO, MIN et Pp.
Rev. hetmat. 5(3-4): 429-432. [3]
MORGANTI, G., PANELLA, I., & CRESSERI, A. Distribution des types Rh dans la population
italienne. Rev. hinat. 5(3-4): 329-333.
MOURANT, A. E. Les groupes sanguins en rapport avec l'anthropologie. Rev. h1mat. 5(3-4):
446. [1]
MULLER, H. J. Some present problems in the genetic effects of radiation. J. Cell. Physiol.
35(Suppl.1): 9-70.
MULLER, H. J. Partial dominance in relation to the need for studying induced mutations
individually. J. Cell. Physiol. 35(Suppl. 1): 205-210.
PENROSE, L. S. Data for the study of linkage in man: red hair and the ABO locus. Ann.
Eugen., Cambr. 15(3): 243-247. [1]
PFXNDLER, U. Quelques mutations affectant les yeuxs, recueillies a titre d'exemples dans
le Canton de Neuchatel et le Jura Bernois (aniridie congenitale, albinisme universel,
abulbie congenitale, achromatopsie totale, oligophrenie associee au keratocone a l'ectopie du cristallin, a la cataracte congenitale et a l'atrophie du nerf optique). Bull.
Schweiz. Akad. med. Wiss., Basel, 6(2): 134-146. [2]
PFXNDLER, U. Eine einfach rezessive Form der Dystrophia musculorum progressiva mit
einer Sippenstammtafel aus dem Emmental (Schweiz). Deut. med. Wschr. 75(37):
1221-1225.
PICHEZZI, L. Determinazione del sesso a volonta. Policlinico. Sez. prat. 57(28): 767-771.
PLANQUES, & RUFFIE, J. L'examen des groupes sanguins dans les proces de filiation. Toulouse med. 51(7): 391-410.
PLATT, R. Heredity. Med. Leg. J., Lond. 18(2): 60-61.
RENTON, P. H., & STRATTON, F. Rhesus type DU. Ann. Eugen., Cambr. 15(3): 189-209.
RITTINEN, P., & BECKER, E. Om tandvaxlingen, kariesfrekvensen, variationerna i tandb&garnas storlek och intermaxillara f6rhallanden samt en del andra iakttagelser hos
finska tvillingar och trillingar. Odont. tskr. 58(1): 33-56.
ROBERTS, J. A. F. The genetics of oligophrenia. Proc. VI Congr. Internat. Psychiat. (Paris,
1950). Paris: Hermann & Cie. Pp. 55-117. [1]
ROBERTS, J. A. F. Eugenics and the influence of heredity. Nurs. Mirror, 91(2368): 363-364.
RYWLIN, A. Recherche de marqueurs de chromosomes dans une famille atteinte de retinite
pigmentaire dominante. Acta genet. 2(1): 1-19. [Clinique Ophtalmologique, Univ.
Geneve, Switz.]
SCHAPER, G. Diskordantes Auftreten spastischer Pylorusstenose bei eineiigen Zwillingen.
Kinderarztl. Prax. 18(5-6): 244-246.
SCHMITZ, K. L. Der K6rperbautyp bei gastrobulbarem Ulcus. Hippokrates, 21(11): 297-298.
SERRA, F. Ricerche eritrocitometriche sui malati di anemia microcitica costituzionale.
Policlinico. Sez. prat. 57(24): 785-789.
SILLEVIS SMITT, W. G., & TRnmos, C. J. Von Recklinghausen's disease in identical twins.
Fol. psychiat. &c. neerl. 53(2): 408-420.

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BIBLIOGRAPHY, 1950, PART 2

SILVESTRONI, E. Emopatie familiari a substrato microcitemico e falcemico. Policlinico. Sez.


prat. 57(26): 841-854. [3]
SIMONS, R. T., & GRAYDON, J. J. Observations on recent discoveries connected with the
blood groups Rh (Cw and DU), M-N (S), Lewis (Le), together with the Rh and M-N
types and agglutinogen P in white Australians. Med. J. Australia, 1(21): 681-688. [2]
SONTAG, L. W. The genetics of differences in psychosomatic patterns in childhood. Am. J.
Orthopsychiat. 20(3): 479-489. [Fels Inst., Yellow Springs, Ohio]
STRANSKU, D. N. Kariesnata problema v svetlinata na nainovite skhvashchaniia po neinata
geneza. (Problem of dental caries from the viewpoint of genetics). Z'bolek. pregl., Sofia,
32(2): 76-84.
SVENDSEN, B. B. Ergebnisse der Erbforschung auf den Gebieten der Oligophrenie, Epilepsie
und anderer neurologischer Krankheiten (1939-1946). Zbl. ges. Neur. Psychiat. 110(1-3):
1-21. [Dept. Med. Genetics, N. Y. State Psychiatric Inst., New York 32, N. Y.]
ULLRICH, 0. Embryo-fetale Hautschwellungen als phanogenetische Gestaltungsfaktoren.
Mschr. Kinderh. 98(10): 416-420. [1]
URECHIA, C. I., RETEZEANO, A., & MALLER, 0. La maladie de Hallervorden-Spatz; deux
cas de rigidite progressive familiale avec un examen anatomique. Encdphale, 39(3):
197-21
VAN CREVELD, S., HOORWEG, P. G., & PAULSSEN, M. M. P. Onderzoekingen over een
circulerend anticoagulans bij een lijder aan haemophilie. Ned. tschr. geneesk. 94(26):
1833-1840. [3]
VAN DER SPEK, L. A. M., & DE KROMME, L. La permeabilite diaplacentaire aux anticorps
Rh et la maladie hemolytique. Rev. hbmat. 5(3-4): 476-481. [De Kromme: 4]
VAN LOGHEm, J. J. JR. Quelques nouveaux aspects des recherches de groupes sanguins.
Bruxelles mtd. 30(35): 1821-1822.
VAN LOGHEm, J. J. JR. Serological investigations of the anti human globulin serum (serum
of Coombs) with special reference to the pathogenesis of erythroblastosis foetalis.
Mschr. kindergeneesk. 18(3-4): 115-126.
VAN LOGHEm, J. J. JR. The difference in the genetic relation of CW to C and c, and DU to
D and d. Mschr. kindergeneesk. 18(3-4): 127-129.
VAN LOGHEm, J. J. JR., Genetique des facteurs Rh. Rev. hemat. 5(3-4): 433-438.
VAN LOGHEM, J. J. JR. Recherches serologiques sur les anticorps immuns anti-Rh. Rev.
hemat. 5(3-4): 439-440.
VAN LOGHEM, J. J. JR., VAN DER HART, M., & PAULUSSEN, A. M. H. Quelques considerations sur la pathogenie de la maladie hemolytique du nouveau-ne, en particulier sur
le m6canisme serologique de l'iso-immunisation par les antigenes A and B. Rev. htmat.
5(3-4): 371-395.
WAARDENBURG, P. J. De incomplete vorm van de aangeboren totale kleurenblindheid.
Ned. tschr. geneesk. 94(18): 1241-1246. [2]
WAARDENBURG, P. J. Twin research in ophthalmology. Docum. ophth. 4(1): 154-199.
WANNER, 0. Genealogische Ueberprufung des Wesens der Geitsesst6rungen bei Hirntumor.
Nervenarzt, 21(6): 252-254.
WESOLOWSKI, S. Okreslanie plci u obojnak6w. (Determination of sex in hermaphroditism).
Polski tygod. lek. 5(7): 260-263.
WIENER, A. S. Reaction transfusionnelle hemolytique due a une sensibilisation anti-M.
ReV. hemat. 5(1): 3-6. [1]
WRIGHT, S. Discussion of population genetics and radiation. J. Cell. Physiol. 35(Suppl. 1):
187-205. [Dept. Zoology, Univ. Chicago, Chicago 37, Ill.]
WRIGHT, S. Genetical structure of populations. Nature, Lond. 166(4215): 247-249.
WRIGHT, S. Genetic structure of populations. Brit. M. J. 2(4669): 36.