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Results: 1-11 |
Results: 11
CLINICAL, MORPHOLOGICAL AND BIOCHEMICAL FEATURES IN THE FAMILIAL ARTICULAR HYPERMOBILITY SYNDROME (FAHS) - A FAMILY STUDY
Authors: GARCIACRUZ D CANOCOLIN S SANCHEZCORONA J GALLEGOS MP CHIMALMONROY J DIAZDELEON L
Citation: D. Garciacruz et al., CLINICAL, MORPHOLOGICAL AND BIOCHEMICAL FEATURES IN THE FAMILIAL ARTICULAR HYPERMOBILITY SYNDROME (FAHS) - A FAMILY STUDY, Clinical genetics, 53(2), 1998, pp. 108-113
CONGENITAL HYPERTRICHOSIS, OSTEOCHONDRODYSPLASIA, AND CARDIOMEGALY - FURTHER DELINEATION OF A NEW GENETIC SYNDROME
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
ASSOCIATION OF LATE-ONSET SPASTIC PARAPARESIS AND DEMENTIA - PROBABLYAN AUTOSOMAL-DOMINANT FORM OF COMPLICATED PARAPLEGIA
Authors: LIZCANOGIL LA GARCIACRUZ D BERNALBELTRAN MDP HERNANDEZ A
Citation: La. Lizcanogil et al., ASSOCIATION OF LATE-ONSET SPASTIC PARAPARESIS AND DEMENTIA - PROBABLYAN AUTOSOMAL-DOMINANT FORM OF COMPLICATED PARAPLEGIA, American journal of medical genetics, 68(1), 1997, pp. 1-6
INTERSTITIAL DELETION 6Q16.2Q22.2 IN A CHILD WITH ECTRODACTYLY
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
MOLECULAR CHARACTERIZATION OF THE FRAGILE-X SYNDROME IN THE MEXICAN POPULATION
Authors: DIAZGALLARDO MY BARROSNUNEZ P DIAZ CA HERNANDEZ A GOMEZESPINEL I LEAL CA FRAGOSO R FIGUERA L GARCIACRUZ D RAMIREZDUENAS ML CANTU JM
Citation: My. Diazgallardo et al., MOLECULAR CHARACTERIZATION OF THE FRAGILE-X SYNDROME IN THE MEXICAN POPULATION, Archives of medical research, 26, 1995, pp. 77-83
PITT-ROGERS-DANKS SYNDROME - FURTHER DELINEATION
Authors: LIZCANOGIL LA GARCIACRUZ D GARCIACRUZ O SANCHEZCORONA J
Citation: La. Lizcanogil et al., PITT-ROGERS-DANKS SYNDROME - FURTHER DELINEATION, American journal of medical genetics, 55(4), 1995, pp. 420-422
CHRISTIANS SPONDYLO-DIGITAL-SYNDROME - 2ND FAMILIAL CASE
Authors: GARCIACRUZ D CANTU JM GARCIAMARTINEZ FJ GARCIACRUZ WO NAZARA Z GONZALEZULLOA B HERNANDEZCORDOVA A RUIZ MX SANCHEZCORONA J
Citation: D. Garciacruz et al., CHRISTIANS SPONDYLO-DIGITAL-SYNDROME - 2ND FAMILIAL CASE, Clinical genetics, 48(5), 1995, pp. 268-271
SPONDYLO-CAMPTODACTYLY SYNDROME - A DISTINCT AUTOSOMAL-DOMINANT ENTITY
Authors: LIZCANOGIL LA GARCIACRUZ D SANCHEZCORONA J CANTU JM
Citation: La. Lizcanogil et al., SPONDYLO-CAMPTODACTYLY SYNDROME - A DISTINCT AUTOSOMAL-DOMINANT ENTITY, Clinical genetics, 48(4), 1995, pp. 173-176
UNEXPECTED FAMILIAL RECURRENCE OF IRIS COLOBOMA - A DELAYED MUTATION MECHANISM
Authors: BARROSNUNEZ P MEDINA C MENDOZA R SANCHEZCORONA J GARCIACRUZ D
Citation: P. Barrosnunez et al., UNEXPECTED FAMILIAL RECURRENCE OF IRIS COLOBOMA - A DELAYED MUTATION MECHANISM, Clinical genetics, 48(3), 1995, pp. 160-161
THE MYHRE SYNDROME - REPORT OF 2 CASES
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
KAUFMAN OCULOCEREBROFACIAL SYNDROME - REPORT OF 2 NEW CASES AND FURTHER DELINEATION
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
Risultati: 1-11 |