AAAAAA

   
Results: 1-14 |
Results: 14
ASSIGNMENT OF GENE RESPONSIBLE FOR PROGRESSIVE PSEUDORHEUMATOID DYSPLASIA TO CHROMOSOME-6 AND EXAMINATION OF COL10A1 AS CANDIDATE GENE
Authors: ELSHANTI H MURRAY JC SEMINA EV BEUTOW KH SCHERPBIER T ALALAMI J
Citation: H. Elshanti et al., ASSIGNMENT OF GENE RESPONSIBLE FOR PROGRESSIVE PSEUDORHEUMATOID DYSPLASIA TO CHROMOSOME-6 AND EXAMINATION OF COL10A1 AS CANDIDATE GENE, European journal of human genetics, 6(3), 1998, pp. 251-256
FANCONIS ANEMIA AND PRIMARY HYPOTHYROIDISM
Authors: ALSHEYYAB M ELSHANTI H GHARIEBEH N EKTIESH F DAOUD AS
Citation: M. Alsheyyab et al., FANCONIS ANEMIA AND PRIMARY HYPOTHYROIDISM, Annals of saudi medicine, 18(1), 1998, pp. 58-59
A RARE CASE OF A LIVEBORN WITH FREE, DE-NOVO AND PARTIAL TRISOMY-12 AND AN UNUSUAL PHENOTYPE
Authors: ELSHANTI H KHASAWNEH M HULSBERG D MAJOR H PATIL S
Citation: H. Elshanti et al., A RARE CASE OF A LIVEBORN WITH FREE, DE-NOVO AND PARTIAL TRISOMY-12 AND AN UNUSUAL PHENOTYPE, Annales de genetique, 40(3), 1997, pp. 175-180
THE ASSIGNMENT OF THE GENE RESPONSIBLE FOR PROGRESSIVE PSEUDORHEUMATOID DYSPLASIA TO THE LONG ARM OF CHROMOSOME-6 AND EXAMINATION OF COL10A1 AS A CANDIDATE GENE
Authors: ELSHANTI H MURRAY J SEMINA E BEUTOW K SCHERPBIER T ALALAMI J ALKHATIB A
Citation: H. Elshanti et al., THE ASSIGNMENT OF THE GENE RESPONSIBLE FOR PROGRESSIVE PSEUDORHEUMATOID DYSPLASIA TO THE LONG ARM OF CHROMOSOME-6 AND EXAMINATION OF COL10A1 AS A CANDIDATE GENE, American journal of human genetics, 61(4), 1997, pp. 1596-1596
AUTOSOMAL RECESSIVE LAMELLAR ICHTHYOSIS AND ACUTE LYMPHOBLASTIC-LEUKEMIA
Authors: ALSHEYYAB M ELSHANTI H TODD D SHURMAN A
Citation: M. Alsheyyab et al., AUTOSOMAL RECESSIVE LAMELLAR ICHTHYOSIS AND ACUTE LYMPHOBLASTIC-LEUKEMIA, European journal of human genetics, 4(2), 1996, pp. 105-107
NEURAL-TUBE DEFECTS IN NORTHERN JORDAN
Authors: DAOUD AS ALKAYSI F ELSHANTI H BATIEHA A OBEIDAT A ALSHEYYAB M
Citation: As. Daoud et al., NEURAL-TUBE DEFECTS IN NORTHERN JORDAN, Saudi medical journal, 17(1), 1996, pp. 78-81
NEONATAL MENINGITIS IN NORTHERN JORDAN
Authors: DAOUD AS ALSHEYYAB M ABUEKTEISH F OBEIDAT A ALI AA ELSHANTI H
Citation: As. Daoud et al., NEONATAL MENINGITIS IN NORTHERN JORDAN, Journal of tropical pediatrics, 42(5), 1996, pp. 267-270
HENOCH-SCHONLEIN PURPURA - CLINICAL-EXPERIENCE AND CONTEMPLATIONS ON A STREPTOCOCCAL ASSOCIATION
Authors: ALSHEYYAB M ELSHANTI H AJLOUNI S BATIEHA A DAOUD AS
Citation: M. Alsheyyab et al., HENOCH-SCHONLEIN PURPURA - CLINICAL-EXPERIENCE AND CONTEMPLATIONS ON A STREPTOCOCCAL ASSOCIATION, Journal of tropical pediatrics, 42(4), 1996, pp. 200-203
THE CLINICAL SPECTRUM OF HENOCH-SCHONLEIN PURPURA IN INFANTS AND YOUNG-CHILDREN
Authors: ALSHEYYAB M ELSHANTI H AJLOUNI S SAWALHA D DAOUD A
Citation: M. Alsheyyab et al., THE CLINICAL SPECTRUM OF HENOCH-SCHONLEIN PURPURA IN INFANTS AND YOUNG-CHILDREN, European journal of pediatrics, 154(12), 1995, pp. 969-972
A CLINICAL-STUDY OF A LARGE INBRED KINDRED WITH AUTOSOMAL RECESSIVE FAMILIAL SPASTIC PARAPLEGIA
Authors: ELSHANTI H DAOUD AS
Citation: H. Elshanti et As. Daoud, A CLINICAL-STUDY OF A LARGE INBRED KINDRED WITH AUTOSOMAL RECESSIVE FAMILIAL SPASTIC PARAPLEGIA, American journal of human genetics, 57(4), 1995, pp. 480-480
MINUTE SUPERNUMERARY RING CHROMOSOME-22 ASSOCIATED WITH CAT EYE SYNDROME - FURTHER DELINEATION OF THE CRITICAL REGION
Authors: MEARS AJ ELSHANTI H MURRAY JC MCDERMID HE PATIL SR
Citation: Aj. Mears et al., MINUTE SUPERNUMERARY RING CHROMOSOME-22 ASSOCIATED WITH CAT EYE SYNDROME - FURTHER DELINEATION OF THE CRITICAL REGION, American journal of human genetics, 57(3), 1995, pp. 667-673
TRANSIENT IMPROVEMENT OF CONGENITAL LACTIC-ACIDOSIS IN A MALE INFANT WITH PYRUVATE DECARBOXYLASE DEFICIENCY TREATED WITH DICHLOROACETATE
Authors: TOTH PP ELSHANTI H EIVINS S RHEAD WJ KLEIN JM
Citation: Pp. Toth et al., TRANSIENT IMPROVEMENT OF CONGENITAL LACTIC-ACIDOSIS IN A MALE INFANT WITH PYRUVATE DECARBOXYLASE DEFICIENCY TREATED WITH DICHLOROACETATE, The Journal of pediatrics, 123(3), 1993, pp. 427-430
A 3 GENERATION MINUTE SUPERNUMARARY RING 22 - ASSOCIATION WITH CAT-EYE SYNDROME
Authors: ELSHANTI H HULSEBERG D MURRAY JC PATIL SR
Citation: H. Elshanti et al., A 3 GENERATION MINUTE SUPERNUMARARY RING 22 - ASSOCIATION WITH CAT-EYE SYNDROME, American journal of human genetics, 53(3), 1993, pp. 126-126
COMBINED MAPPING APPROACHES TO RIEGER SYNDROME
Authors: MURRAY J ELSHANTI H LINDGREN C LEYSENS N PATIL S ZABEL B ALWARD W STEVENSON T BITOUN P BUETOW K
Citation: J. Murray et al., COMBINED MAPPING APPROACHES TO RIEGER SYNDROME, American journal of human genetics, 53(3), 1993, pp. 141-141
Risultati: 1-14 |