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Results:
1-16
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Results: 16
Authors:
LEAL CA
AYALAMADRIGAL ML
FIGUERA LE
MEDINA C
Citation: Ca. Leal et al., HISTONE H4 ACETYLATION ANALYSES IN PATIENTS WITH POLYSOMY X - IMPLICATIONS FOR THE MECHANISM OF X-INACTIVATION, Human genetics, 103(1), 1998, pp. 29-33
Authors:
CANTU JM
DIAZGALLARDO MY
BARROSNUNEZ P
FIGUERA LE
Citation: Jm. Cantu et al., HETEROALLELIC MONOZYGOTIC TWINS AND TRIPLETS, American journal of medical genetics, 77(2), 1998, pp. 166-167
Authors:
GALLEGOSARREOLA MP
GONZALEZNORIEGA A
ZUNIGAGONZALEZ GM
FLORESMARTINEZ SE
MOGUEL MCM
FIGUERA LE
SANCHEZCORONA J
Citation: Mp. Gallegosarreola et al., MUCOPOLYSACCHARIDOSES TYPE-II - ENZYMATIC-ACTIVITY AND QUANTITATIVE AND QUALITATIVE STUDIES OF URINARY GLYCOSAMINOGLYCANS IN 5 PATIENTS, Archives of medical research, 28(1), 1997, pp. 91-94
Authors:
GARCIACRUZ D
SANCHEZCORONA J
NAZARA Z
GARCIACRUZ MO
FIGUERA LE
CASTANEDA V
CANTU JM
Citation: D. Garciacruz et al., CONGENITAL HYPERTRICHOSIS, OSTEOCHONDRODYSPLASIA, AND CARDIOMEGALY - FURTHER DELINEATION OF A NEW GENETIC SYNDROME, American journal of medical genetics, 69(2), 1997, pp. 138-151
Authors:
YANG SP
BIDICHANDANI SI
FIGUERA LE
JUYAL RC
SAXON PJ
BALDINI A
PATEL PI
Citation: Sp. Yang et al., MOLECULAR ANALYSIS OF DELETION (17)(P11.2P11.2) IN A FAMILY SEGREGATING A 17P PARACENTRIC INVERSION - IMPLICATIONS FOR CARRIERS OF PARACENTRIC INVERSIONS, American journal of human genetics, 60(5), 1997, pp. 1184-1193
Authors:
FIGUERA LE
Citation: Le. Figuera, GELEOPHYSIC DYSPLASIA VS MYHRE SYNDROME, American journal of medical genetics, 65(4), 1996, pp. 361-361
Authors:
CORREACERRO L
GARCIACRUZ D
DIAZCASTANOS L
FIGUERA LE
SANCHEZCORONA J
Citation: L. Correacerro et al., INTERSTITIAL DELETION 6Q16.2Q22.2 IN A CHILD WITH ECTRODACTYLY, Annales de genetique, 39(2), 1996, pp. 105-109
Authors:
JUYAL RC
FIGUERA LE
HAUGE X
ELSEA SH
LUPSKI JR
GREENBERG F
BALDINI A
PATEL PI
Citation: Rc. Juyal et al., MOLECULAR ANALYSES OF 17P11.2 DELETIONS IN 62 SMITH-MAGENIS SYNDROME PATIENTS, American journal of human genetics, 58(5), 1996, pp. 998-1007
Authors:
FIGUERA LE
PANDOLFO M
DUNNE PW
CANTU JM
PATEL PI
Citation: Le. Figuera et al., MAPPING OF THE CONGENITAL GENERALIZED HYPERTRICHOSIS LOCUS TO CHROMOSOME XQ24-Q27.1, Nature genetics, 10(2), 1995, pp. 202-207
Authors:
FIGUERA LE
RAMIREZDUENAS ML
GALLEGOSARREOLA MP
CANTU JM
Citation: Le. Figuera et al., SPONDYLOEPIMETAPHYSEAL DYSPLASIA (SEMD) SHOHAT TYPE, American journal of medical genetics, 51(3), 1994, pp. 213-215
Authors:
FIGUERA LE
CANTU JM
Citation: Le. Figuera et Jm. Cantu, AMBRAL SYNDROME AND CONGENITAL GENERALIZED HYPERTRICHOSIS, Clinical genetics, 46(5), 1994, pp. 384-384
Authors:
FIGUERA LE
JIMENEZGIL FJ
GARCIACRUZ MO
CANTU JM
Citation: Le. Figuera et al., SCHWARTZ-JAMPEL SYNDROME - AN ATYPICAL FORM, American journal of medical genetics, 47(4), 1993, pp. 526-528
Authors:
FIGUERA LE
RIVAS F
CANTU JM
Citation: Le. Figuera et al., ORAL-FACIAL-DIGITAL SYNDROME WITH FIBULAR APLASIA - A NEW VARIANT, Clinical genetics, 44(4), 1993, pp. 190-192
Authors:
GARCIACRUZ D
FIGUERA LE
FERIAVELAZCO A
SANCHEZCORONA J
GARCIACRUZ MO
RAMIREZDUENAS RM
HERNANDEZCORDOVA A
RUIZ MX
BITARALATORRE WE
RAMIREZDUENAS ML
CANTU JM
Citation: D. Garciacruz et al., THE MYHRE SYNDROME - REPORT OF 2 CASES, Clinical genetics, 44(4), 1993, pp. 203-207
Authors:
FIGUERA LE
GARCIACRUZ D
RAMIREZUENAS ML
RIVERAROBLES V
CANTU JM
Citation: Le. Figuera et al., KAUFMAN OCULOCEREBROFACIAL SYNDROME - REPORT OF 2 NEW CASES AND FURTHER DELINEATION, Clinical genetics, 44(2), 1993, pp. 98-101
Authors:
FIGUERA LE
RAMIREZDUENAS M
CANTU JM
Citation: Le. Figuera et al., GUADALAJARA CAMPTODACTYLY SYNDROME TYPE-III, American journal of human genetics, 53(3), 1993, pp. 429-429
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