SCOOTER82a_Livingstone_Frequencies of Hemoglobin Variants ...
SCOOTER82a_Livingstone_Frequencies of Hemoglobin Variants ...
SCOOTER82a_Livingstone_Frequencies of Hemoglobin Variants ...
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
514<br />
Ann Intern Med 98:933-936<br />
1776 Sanghvi LD (1962) <strong>Hemoglobin</strong> survey <strong>of</strong> Maharashtra. Lecture, Department <strong>of</strong> Human Genetics, University <strong>of</strong> Michigan.<br />
i777 Sanna G, Frau F, Virgiliis S de, Plu P, Bertollno F, Cao A (i981) Glucose-6-phosphate dehydrogenase red blood cell<br />
phenotype ln Gd(Mediterranean) heterozygous females ahd hemizygous males at birth. Pedlatr Res i5:1443-1446<br />
1778 Sanna G. Virgiliis S de, Palmas C, Argiolu F, Frau F, Cao A (1979) Favlsm in Gd(Mediterranean) heterozygous females.<br />
Pediatr Res 13:812-816<br />
1779 Sansarricq H, Marill G, Portier A, Cabannes R (i959) Les hemoglobinopathies en Haute-Volta. Sang 30:503-511<br />
1780 Sansone G, Perroni L, Yoshlda A (1975) Glucose-6-phosphate dehydrogenase variants from Italian sUbjects associated with<br />
severe neonatal jaundice. Br J Haematol 31:159-165<br />
1781 Sansone G, Pik C (1965) Familial haemolytic anaemia, with erythrocyte inclusion bodies, bilifuscinuria. and abnormal<br />
haemoglobin (haemoglobin Galliera Genova). Br J Haematol 11:51i-517<br />
1782 Sansone G, Sciarratta GV, Agostl-Vallerlno S, Ivldl G, Parodi MI, Leone-Da Passano 0 (i982) Geographic distribution and<br />
heterogeneity <strong>of</strong> thalassemias in the Italian population. In A Cao, U Carcassi, PT Rowley (Eds), Thalassemia: Recent advances<br />
in detection and treatment. Birth Defects: Original Article Series 18(7):i89-i93<br />
1783 Sansone G, Segni G, Cecco C de (1958) 11 difetto biochimico eritrocitario predisponente all'emolisi favica. Prime<br />
recerche sulla popolazione Ligure e su quella Sarda. Boll Soc Ital Bioi Speriment 34:1558-i56i<br />
1784 Santiago-Borrero PJ, Valcarcel M, Caceres de Costas M, Montalvo F (1983) Geographic distribution <strong>of</strong> abnormal hemoglobins<br />
in Puerto Rico. Bol Asoc Med P Rico 75:447-451<br />
1785 Santos David J, Moura Pires F, Trincao C (1962) Abnormal haemoglobins in the District <strong>of</strong> Lunda and the neighbouring<br />
District <strong>of</strong> Songo, Angola. Man 62:48<br />
1786 Santos David JH (1960) A Drepanocitemia e a Antropologia. Companhia de Diamantes de Angola, Publicacoes Culturals No 49.<br />
(Lisbon)<br />
1787 Santos David JH (1965) A deficiencia da deidrogenase de glucose-6-fosfato (G-6-PD) nos eritrocitos dos nativos da Lunda<br />
e Songo (Angola). Arquivo Anat Antropol 33:141-152<br />
1788 Santos Davis JH, Trincao C (1963) Drepanocitemia, deficiencia de desidrogenase da glucose-6-fosfato (G-6-PD)<br />
ertrocitaria e paludismo no posto do Cuango (Lunda-Angola). An Inst Med Trop Lisboa 20:5-16<br />
1789 Saoji AM. Kelkar SS (1983) Erythrocyte glucose-6-phosphate dehydrogenase isoenzyme phenotypes in leprosy. Inter'nat J<br />
Leprosy 51:41-44<br />
1790 Sar A van der (1949) De sikklecelziekte. Nederl Tijd Geneesk 93:1867-i874<br />
1791 Sar A van der (1959) The occurrence <strong>of</strong> carriers <strong>of</strong> abnormal haemoglobins Sand C on Curacao. Thesis, University <strong>of</strong><br />
Groningen.<br />
1792 Sar A van der, Schouten H, Struyker Boudier AM (1964) Glucose-6-phosphate dehydrogenase deficiency in red cells.<br />
Incidence in the Curacao population, its clinical and genetic aspects. Enzymol 27:289-310<br />
1793 Sarmento A (1944) Contribuicao para 0 estudo da anemia de celulas falciformes nos negros de Angola. An Inst Med Trop<br />
Lisboa 1:345-350<br />
1794 Sarrouy Ch, Cabannes R, Zevaco P (1955) La thalassemie de 1 'enfant indigene nor-africain. Toulouse Med 56:195-219<br />
1795 Satoh C, Neel JV, Yamashita A, Goriki K, FUjita M, Hamilton HB (1983) The frequency among Japanese <strong>of</strong> heterozygotes for<br />
deficiency variants <strong>of</strong> 11 enzymes. Am J Hum Genet 35:656-674<br />
1796 Saugrain J (1957) Nouvelles recherches sur la drepanocytose a Madagascar. Bull Soc Pathol Exot 50:480-486<br />
1797 Say B, Ozand P, Berkell I, Cevk N (1965) Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Turkey. Acta<br />
Paediatr Scand 54:319-324<br />
1798 Sayed BA, Amin SP (1966) A survey <strong>of</strong> sickle cell trait in Bhi.l tribe in Baroda District along with blood group data. J<br />
J.v. Group <strong>of</strong> Hosp Grant Med College, Bombay, 11:169-171<br />
1799 Scappaticci E, Miniero R, Torta F, David 0, Massaro AL, Saglio G, Palestro M, Nicola P (1975) Frequenza del tratto<br />
talassemico e del deficit de G-6-PO nella popolazione scolastica di Comuni della "Cintura" Torinese. Min Pediatr 27:419-425<br />
1800 Schiliro G (i978) Sicily: the world reservoir for thalassemias and haemoglobinopathies. Nature 276:76i<br />
1801 Schiliro G, Musumeci S, Pizzarelli G, DiGregorio L, Fischer A, Russo G (1978) Beta-thalassemia in Sicily. Hematological<br />
and biosynthetic studies. Acta Haematol 60:193-200<br />
1802 Schiliro G. Russo A, Curreri R, Marino S, Sciotto A, Russo G (1979) Glucose-6-phosphate dehydrogenase deficiency in<br />
Sicily. Incidence, biochemical characteristics and clinical implications. Clin Genet 15:183-188<br />
1803 Schiliro G, Russo A, Di Gregorio F, Musumeci S (1976) Thalassaemia in Italy. Lancet 1:598<br />
1804 Sch1zas N, Tegos K, Voutsadakis A, Arabatzis G, Agelopoulou P, Chrysanthopoulos K, Athanasiadou A, Bathrelou S, Robos J,<br />
Skarlos D, Davakis M (1977) The frequency and dlstribution <strong>of</strong> beta-thalassaemia and abnormal haemogloblns in Greece. A study<br />
on 15,550 recruits. Hellenic Armed Forces Med Rev, Suppl I (Athens) 11:197-209 (In Greek)<br />
1805 Schneer JH (i968) A survey for erythrocyte glucose-6-phosphate dehydrogenase deficiency in Rumania. Acta Haematol<br />
40:44-47<br />
1806 Schneider P, Anantha Krishnan R, Walter H, Xirotiris N, Abele R (1975) Enzyme polymorphism and haemoglobin varlants ln<br />
Greeks. Humangenetlk 27:217-222<br />
1807 Schneider RG (1954) Incidence <strong>of</strong> hemoglobin C trait in 505 normal Negroes. A family with homozygous hemoglobin C and<br />
sickle-cell trait union. v Lab Clin Med 44:133-144