ACCUMULATION OF CARBON DIOXIDE IN OXYGEN HOODS, INFANT COTS, AND INCUBATORS.GALE R; REDNER CARMI R; GALE J et al.1977; PEDIATRICS; U.S.A.; DA. 1977; VOL. 60; NO 4 PART. 1; PP. 453-456; BIBL. 15 REF.Article

THE BRANCHIO-OTO-RENAL (BOR) SYNDROME: REPORT OF BILATERAL RENAL AGENESIS IN THREE SIBSCARMI R; BINSHTOCK M; ABELIOVICH D et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 4; PP. 625-627; BIBL. 10 REF.Article

Pentalogy of cantrell and associated midline anomalies : a possible ventral midline development fieldCARMI, R; BOUGHMAN, J. A.American journal of medical genetics. 1992, Vol 42, Num 1, pp 90-95, issn 0148-7299Article

The snowflake sign : a sonographic marker for prenatal detection of fetal skin denudationMEIZNER, I; CARMI, R.Journal of ultrasound in medicine. 1990, Vol 9, Num 10, pp 607-609, issn 0278-4297Article

Human values in urban architecture in New trends in urban planning. Studies in housing, urban design and planningCARMI, R; SOEN, D.International symposium. 1979, pp 159-175, isbn 0-08-024266-9, isbn 0-08-024266-9Conference Proceedings

Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43PARVARI, R; HERSHKOVITZ, E; KANIS, A et al.American journal of human genetics. 1998, Vol 63, Num 1, pp 163-169, issn 0002-9297Article

Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim ArabPARVARI, R; MOSES, S; HERSHKOVITZ, E et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 1, pp 21-27, issn 0141-8955Article

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mappingSHEFFIELD, V. C; CARMI, R; KWITEK-BLACK, A et al.Human molecular genetics (Print). 1994, Vol 3, Num 8, pp 1331-1335, issn 0964-6906Article

The thoracoabdominal syndrome (TAS) : a new ×-linked dominant disorderCARMI, R; BARBASH, A; MARES, A. J et al.American journal of medical genetics. 1990, Vol 36, Num 1, pp 109-114, issn 0148-7299, 6 p.Article

In utero prenatal diagnosis of Beckwith-Wiedemann syndrome; a case reportMEIZNER, I; CARMI, R; KATZ, M et al.European journal of obstetrics, gynecology, and reproductive biology. 1989, Vol 32, Num 3, pp 259-264, issn 0301-2115, 6 p.Article

Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiencyLEIBERMAN, E; PESLER, D; PARVARI, R et al.American journal of medical genetics. 2000, Vol 90, Num 3, pp 188-192, issn 0148-7299Article

Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowthPARVARI, R; MUMM, S; GALIL, A et al.American journal of medical genetics. 1999, Vol 83, Num 4, pp 302-307, issn 0148-7299Article

Clinical presentation and outcome in primary familial hypomagnesaemiaSHALEV, H; PHILLIP, M; GALIL, A et al.Archives of disease in childhood. 1998, Vol 78, Num 2, pp 127-130, issn 0003-9888Article

Linkage of infantile bartter syndrome with sensorineural deafness to chromosome 1pBRENNAN, T. M. H; LANDAU, D; SHALEV, H et al.American journal of human genetics. 1998, Vol 62, Num 2, pp 355-361, issn 0002-9297Article

Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)PARVARI, R; HERSHKOVITZ, E; CARMI, R et al.Prenatal diagnosis. 1996, Vol 16, Num 9, pp 862-865, issn 0197-3851Article

Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25-26PARVARI, R; WEINSTEIN, Y; EHRLICH, S et al.American journal of medical genetics. 1994, Vol 49, Num 4, pp 431-434, issn 0148-7299Article

Prenatal ultrasound diagnosis of complete absence of the lumbar spine and sacrumMEIZNER, I; PRESS, F; JAFFE, A et al.Journal of clinical ultrasound. 1992, Vol 20, Num 1, pp 77-80, issn 0091-2751Article

Spontaneous resolution of isolated fetal ascites associated with extralobar lung sequestrationMEIZNER, I; CARMI, R; MARES, A. J et al.Journal of clinical ultrasound. 1990, Vol 18, Num 1, pp 57-60, issn 0091-2751Article

Persistent hyperinsulinemic hypoglycemia of infancy 'nesidioblastosis : autosomal recessive inheritance in 7 pedigreesGLASER, B; PHILLIP, M; CARMI, R et al.American journal of medical genetics. 1990, Vol 37, Num 4, pp 511-515, issn 0148-7299Article

Osteopetrosis : a single centre experience of stem cell transplantation and prenatal diagnosisKAPELUSHNIK, J; SHALEV, C; YANIV, I et al.Bone marrow transplantation (Basingstoke). 2001, Vol 27, Num 2, pp 129-132, issn 0268-3369Article

Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita : Histopathological delineation of an autosomal recessive diseaseMAMAN, E; MAOR, E; KACHKO, L et al.American journal of medical genetics. 1998, Vol 78, Num 2, pp 127-133, issn 0148-7299Article

Use of isolated inbred human populations for identification of disease genesSHEFFIELD, V. C; STONE, E. M; CARMI, R et al.Trends in genetics (Regular ed.). 1998, Vol 14, Num 10, pp 391-396, issn 0168-9525Article

Endocardial cushion defect : further studies of isolated versus syndromic occurrenceCARMI, R; BOUGHMAN, J. A; FERENCZ, C et al.American journal of medical genetics. 1992, Vol 43, Num 3, pp 569-575, issn 0148-7299Article

Early prenatal ultrasound diagnosis of thanatophoric dwarfismMEIZNER, I; CARMI, R; LEVY, A et al.Israel journal of medical sciences. 1990, Vol 26, Num 5, pp 287-289, issn 0021-2180Article

A case of ambiguous genitalia owing to neurofibromatosis ― review of the literatureKANETI, J; LIEBERMAN, E; MOSHE, P et al.The Journal of urology. 1988, Vol 140, Num 3, pp 584-585, issn 0022-5347Article