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COMPUTER-ASSISTED ANALYSIS OF CHROMOSOMAL ABNORMALITIES: DETECTION OF A DELETION IN ANIRIDIA/WILMS'TUMOR SYNDROME = ANALYSE A L'AIDE D'ORDINATEUR D'ANOMALIES CHROMOSOMIQUES: DETECTION D'UNE DELETION DANS LE SYNDROME ANIRIDIE/TUMEURS DE WILMSLADDA R; ATKINS L; LITTLEFIELD J et al.1974; SCIENCE; U.S.A.; DA. 1974; VOL. 185; NO 4153; PP. 784-787; BIBL. 13REF.Article

LONG-TERM PERSISTENCE OF CYTOMEGALOVIRUS GENOME IN CULTURED HUMAN CELLS OF PROSTATIC ORIGIN. = LONGUE PERSISTANCE DU GENOME DU CYTOMEGALOVIRUS DANS DES CULTURES DE CELLULES DE PROSTATE HUMAINERAPP F; GEDER L; MURASKO D et al.1975; J. VIROL.; U.S.A.; DA. 1975; VOL. 16; NO 4; PP. 982-990; BIBL. 22 REF.Article

Protein kinase C and non-functional EGF receptor in K-ras transformed cellsCHU CHANG CHUA; LADDA, R. L.Biochemical and biophysical research communications (Print). 1986, Vol 135, Num 2, pp 435-444, issn 0006-291XArticle

Generalized epidermolytic hyperkeratosis in the child of a parent with nevus comedonicusLOOKINGBILL, D. P; LADDA, R. L; COHEN, C et al.Archives of dermatology (1960). 1984, Vol 120, Num 2, pp 223-226, issn 0003-987XArticle

A new family of functional series relations involving digamma functionsRAINA, R. K; LADDA, R. K.Annales mathématiques Blaise Pascal. 1996, Vol 3, Num 2, pp 189-198, issn 1259-1734Article

ESTABLISHMENT AND CHARACTERIZATION OF A NEW HUMAN URINARY BLADDER CARCINOMA CELL LINE (PS-1)SANFORD EJ; GEDER L; DAGEN JE et al.1978; INVEST. UROL.; USA; DA. 1978; VOL. 16; NO 3; PP. 246-252; BIBL. 22 REF.Article

Ocular findings in patients with cerebroocular dysplasia-muscular dystrophy syndromeSASSANI, J. W; TOWFIGHI, J; LADDA, R. L et al.Annals of ophthalmology (Birmingham). 1994, Vol 26, Num 6, pp 225-235, issn 0003-4886Article

Cerebro-ocular dysplasia - muscular dystrophy (Walker Warburg) syndrome. Findings in 20-week-old fetusMILLER, G; LADDA, R. L; TOWFIGHI, J et al.Acta neuropathologica. 1991, Vol 82, Num 3, pp 234-238, issn 0001-6322Article

Effect of tunicamycin on the biosynthesis of human fibroblast collagenaseCHU CHANG CHUA; LADDA, R. L.Collagen and related research. 1987, Vol 7, Num 4, pp 285-293, issn 0174-173XArticle

Two infants with del(3)(p25pter) and a review of previously reported casesRAMER, J. C; LADDA, R. L; FRANKEL, C et al.American journal of medical genetics. 1989, Vol 33, Num 1, pp 108-112, issn 0148-7299Article

Malformations in a child with dup (7 pter-p1501) and del (7 q36-qter) as a result of familial pericentric inversionRAMER, J. C; MOWREY, P. N; LADDA, R. L et al.Clinical genetics. 1991, Vol 39, Num 6, pp 442-450, issn 0009-9163, 9 p.Article

Multiple Pterygium syndrome: an overviewRAMER, J. C; LADDA, R. L; DEMUTH, W. W et al.American journal of diseases of children (1960). 1988, Vol 142, Num 7, pp 794-798, issn 0002-922XArticle

Dandy-Walker malformation in Ellis-van Creveld syndromeZANGWILL, K. M; BOAL, D. K. B; LADDA, R. L et al.American journal of medical genetics. 1988, Vol 31, Num 1, pp 123-129, issn 0148-7299Article

Marden-Walker phenotype : spectrum of variability in three infantsRAMER, J. C; FRANKEL, C. A; LADDA, R. L et al.American journal of medical genetics. 1993, Vol 45, Num 3, pp 285-291, issn 0148-7299Article

Receptor for epidermal growth factor retains normal structure and function in aging cellsCHU CHANG CHUA; GEIMAN, D. E; LADDA, R. L et al.Mechanisms of ageing and development. 1986, Vol 34, Num 1, pp 35-55, issn 0047-6374Article

Cerebro-ocular-dysplasia-Muscular dystrophy (COD-MD) syndromeTOWFIGHI, J; SASSANI, J. W; SUZUKI, K et al.Acta neuropathologica. 1984, Vol 65, Num 2, pp 110-123, issn 0001-6322Article

Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment : a distinct syndromeLADDA, R. L; ZONANA, J; RAMER, J. C et al.American journal of medical genetics. 1993, Vol 47, Num 4, pp 550-555, issn 0148-7299Article

Neurologic manifestations in 18q- syndromeMILLER, G; MOWREY, P. N; HOPPER, K. D et al.American journal of medical genetics. 1990, Vol 37, Num 1, pp 128-132, issn 0148-7299, 5 p.Article

Induction and suppression of type I collagenase in cultured human cellsCHU CHANG CHUA; BARRITAULT, D; GEIMAN, D. E et al.Collagen and related research. 1987, Vol 7, Num 4, pp 277-284, issn 0174-173XArticle

Encouraging patients to undergo prenatal genetic counseling before the day of amniocentesis. Its effect on the use of amniocentesisLORENZ, R. P; BOTTI, J. J; SCHMIDT, C. M et al.Journal of reproductive medicine. 1985, Vol 30, Num 12, pp 933-935, issn 0024-7758Article

Inheritance of an RNA splicing mutation (G^+1IVS20) in the type III procollagen gene (COL3Al) in a family having aortic aneurysms and easy bruisability : phenotypic overlap between familial arterial aneurysms and Ehlers-Danlos syndrome type IVKONTUSAARI, S; TROMP, G; KUIVANIEMI, H et al.American journal of human genetics. 1990, Vol 47, Num 1, pp 112-120, issn 0002-9297, 9 p.Article

Induction of collagenase secretion in human fibroblast cultures by growth promoting factorsCHU CHANG CHUA; GEIMAN, D. E; KELLER, G. H et al.The Journal of biological chemistry (Print). 1985, Vol 260, Num 9, pp 5213-5216, issn 0021-9258Article

Cutaneous scar at anterior hair line in mother and child with associated frontal bone defect in childSTRATIS, J. P; RAMER, J. C; MANDERS, E. K et al.American journal of medical genetics. 1992, Vol 44, Num 2, pp 197-199, issn 0148-7299Article

Previously apparently undescribed syndrome : shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardationRAMER, J. C; LIN, A. E; DOBYNS, W. B et al.American journal of medical genetics. 1995, Vol 57, Num 3, pp 403-409, issn 0148-7299Article