RELATIVE LEVELS OF METHYLATION IN HUMAN GROWTH HORMONE AND CHORIONIC SOMATOMAMMOTROPIN GENES IN EXPRESSING AND NON-EXPRESSING TISSUESHJELLE BL; PHILLIPS JA III; SEEBURG PH et al.1982; NUCLEIC ACIDS RES.; ISSN 0305-1048; GBR; DA. 1982; VOL. 10; NO 11; PP. 3459-3474; BIBL. 38 REF.Article

ANALYSIS OF GROWTH HORMONE GENES IN MICE WITH GENETIC DEFECTS OF GROWTH HORMONE EXPRESSIONPHILLIPS JA III; BEAMER WG; BARTKE A et al.1982; J. ENDOCRINOL.; ISSN 0022-0795; GBR; DA. 1982; VOL. 92; NO 3; PP. 405-407; H.T. 1; BIBL. 16 REF.Article

HEMOGLOBIN H DISEASE AND MULTIPLE CONGENITAL ANOMALIES IN A CHILD OF NORTHERN EUROPEAN ORIGINHJELLE B; CHARACHE S; PHILLIPS JA III et al.1982; AMERICAN JOURNAL OF HEMATOLOGY; ISSN 0361-8609; USA; DA. 1982; VOL. 13; NO 4; PP. 319-322; BIBL. 7 REF.Article

GENETIC DISEASES: DIAGNOSIS BY RESTRICTION ENDONUCLEASE ANALYSISANTONARAKIS SE; PHILLIPS JA III; KAZAZIAN HH JR et al.1982; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1982; VOL. 100; NO 6; PP. 845-856; BIBL. 76 REF.Article

THE GENES FOR GROWTH HORMONE AND CHORIONIC SOMATOMAMMOTROPIN ARE ON THE LONG ARM OF HUMAN CHROMOSOME 17 IN REGION Q21->QTERGEORGE DL; PHILLIPS JA III; FRANCKE U et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 2; PP. 138-141; BIBL. 29 REF.Article

A MOLECULAR BASIS FOR HEMOGLOBIN-H DISEASE IN AMERICAN BLACKSPHILLIPS JA III; SCOTT AF; SMITH KD et al.1979; BLOOD; USA; DA. 1979; VOL. 54; NO 6; PP. 1439-1445; BIBL. 20 REF.Article

THE MOLECULAR BASIS OF HEMOGLOBIN GRADYSCOTT AF; PHILLIPS JA III; YOUNG KE et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 1; PP. 129-133; BIBL. 12 REF.Article

PRENATAL DIAGNOSIS OF BETA -THALASSEMIAS BY AMNIOCENTESIS LINKAGE ANALYSIS USING MULTIPLE POLYMORPHIC RESTRICTION ENDONUCLEASE SITESKAZAZIAN HH JR; PHILLIPS JA III; BOEHM CD et al.1980; BLOOD; ISSN 0006-4971; USA; DA. 1980; VOL. 56; NO 5; PP. 926-930; BIBL. 21 REF.Article

GENETIC ANALYSIS OF FAMILIAL ISOLATED GROWTH HORMONE DEFICIENCY TYPE IPHILLIPS JA III; PARKS JS; HJELLE BL et al.1982; JOURNAL OF CLINICAL INVESTIGATION; ISSN 0021-9738; USA; DA. 1982; VOL. 70; NO 3; PP. 489-495; BIBL. 25 REF.Article

PRENATAL DIAGNOSIS OF HEMOGLOBINOPATHIES BY RESTRICTION ENDONUCLEASE ANALYSIS: PREGNANCIES AT RISK FOR SICKLE CELL ANEMIA AND S-O ARAL DISEASEPHILLIPS JA III; SCOTT AF; KAZAZIAN HH JR et al.1979; JOHNS HOPKINS MED. J.; USA; DA. 1979; VOL. 145; NO 2; PP. 57-60; BIBL. 20 REF.Article

POPULATION HETEROGENEITY OF THE HPAI RESTRICTION SITE ASSOCIATED WITH THE BETA GLOBIN GENE: IMPLICATIONS FOR PRENATAL DIAGNOSISPANNY SR; SCOTT AF; SMITH KD et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 1; PP. 25-35; BIBL. 27 REF.Article

UNEQUAL CROSSING-OVER: A COMMON BASIS OF SINGLE ALPHA -GLOBIN GENES IN ASIANS AND AMERICAN BLACKS WITH HEMOGLOBIN-H DISEASEPHILLIPS JA III; VIK TA; SCOTT AF et al.1980; BLOOD; USA; DA. 1980; VOL. 55; NO 6; PP. 1066-1069; BIBL. 12 REF.Article

PRENATAL DIAGNOSIS OF LETHAL PERINATAL OSTEOGENESIS IMPERFECTA (OI TYPE II)SHAPIRO JE; PHILLIPS JA III; BYERS PH et al.1982; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1982; VOL. 100; NO 1; PP. 127-133; BIBL. 25 REF.Article