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Results: 1-18 |
Results: 18
SMITH-FINEMAN-MYERS-SYNDROME IN APPARENTLY MONOZYGOTIC TWINS
Authors: GUIONALMEIDA ML TABITH A KOKITSUNAKATA NM ZECHI RM
Citation: Ml. Guionalmeida et al., SMITH-FINEMAN-MYERS-SYNDROME IN APPARENTLY MONOZYGOTIC TWINS, American journal of medical genetics, 79(3), 1998, pp. 205-208
BLEPHARO-CHEILO-DONTIC (BCD) SYNDROME - REPORT ON 4 NEW PATIENTS
Authors: GUIONALMEIDA ML RODINI ESO KOKITSUNAKATA NM BOLOGNAAMANTINI D
Citation: Ml. Guionalmeida et al., BLEPHARO-CHEILO-DONTIC (BCD) SYNDROME - REPORT ON 4 NEW PATIENTS, American journal of medical genetics, 76(2), 1998, pp. 133-136
OCULOAURICULOFRONTONASAL SPECTRUM IN AN ADULT BRAZILIAN MALE
Authors: GUIONALMEIDA ML LOPES VLGS
Citation: Ml. Guionalmeida et Vlgs. Lopes, OCULOAURICULOFRONTONASAL SPECTRUM IN AN ADULT BRAZILIAN MALE, Clinical dysmorphology, 6(3), 1997, pp. 251-255
OHDO-SYNDROME - REPORT ON A BRAZILIAN GIRL WITH ADDITIONAL FINDINGS
Authors: LOPES VLGD GUIONALMEIDA ML
Citation: Vlgd. Lopes et Ml. Guionalmeida, OHDO-SYNDROME - REPORT ON A BRAZILIAN GIRL WITH ADDITIONAL FINDINGS, Clinical genetics, 51(4), 1997, pp. 268-270
FRONTONASAL DYSPLASIA - ANALYSIS OF 21 CASES AND LITERATURE-REVIEW
Authors: GUIONALMEIDA ML RICHIERICOSTA A SAAVEDRA D COHEN MM
Citation: Ml. Guionalmeida et al., FRONTONASAL DYSPLASIA - ANALYSIS OF 21 CASES AND LITERATURE-REVIEW, International journal of oral and maxillofacial surgery, 25(2), 1996, pp. 91-97
CRANIOFRONTONASAL SYNDROME - STUDY OF 41 PATIENTS
Authors: SAAVEDRA D RICHIERICOSTA A GUIONALMEIDA ML COHEN MM
Citation: D. Saavedra et al., CRANIOFRONTONASAL SYNDROME - STUDY OF 41 PATIENTS, American journal of medical genetics, 61(2), 1996, pp. 147-151
CEREBROFACIOTHORACIC SYNDROME
Authors: GUIONALMEIDA ML RICHIERICOSTA A SAAVEDRA D COHEN MM
Citation: Ml. Guionalmeida et al., CEREBROFACIOTHORACIC SYNDROME, American journal of medical genetics, 61(2), 1996, pp. 152-153
DELLEMAN SYNDROME IN A BRAZILIAN BOY
Authors: GUIONALMEIDA ML KOKITSUNAKATA NM
Citation: Ml. Guionalmeida et Nm. Kokitsunakata, DELLEMAN SYNDROME IN A BRAZILIAN BOY, Brazilian journal of genetics, 19(4), 1996, pp. 625-627
OPITZ-SYNDROME IS GENETICALLY HETEROGENEOUS, WITH ONE LOCUS ON XP22, AND A 2ND LOCUS ON 22Q11.2
Authors: ROBIN NH FELDMAN GJ ARONSON AL MITCHELL HF WEKSBERG R LEONARD CO BURTON BK JOSEPHSON KD LAXOVA R ALECK KA ALLANSON JE GUIONALMEIDA ML MARTIN RA LEICHTMAN LG PRICE RA OPITZ JM MUENKE M
Citation: Nh. Robin et al., OPITZ-SYNDROME IS GENETICALLY HETEROGENEOUS, WITH ONE LOCUS ON XP22, AND A 2ND LOCUS ON 22Q11.2, Nature genetics, 11(4), 1995, pp. 459-461
HYPERTELORISM - INTERORBITAL GROWTH, MEASUREMENTS, AND PATHOGENETIC CONSIDERATIONS
Authors: COHEN MM RICHIERICOSTA A GUIONALMEIDA ML SAAVEDRA D
Citation: Mm. Cohen et al., HYPERTELORISM - INTERORBITAL GROWTH, MEASUREMENTS, AND PATHOGENETIC CONSIDERATIONS, International journal of oral and maxillofacial surgery, 24(6), 1995, pp. 387-395
APPARENT MALPUECH-SYNDROME - REPORT ON 3 BRAZILIAN PATIENTS WITH ADDITIONAL SIGNS
Authors: GUIONALMEIDA ML
Citation: Ml. Guionalmeida, APPARENT MALPUECH-SYNDROME - REPORT ON 3 BRAZILIAN PATIENTS WITH ADDITIONAL SIGNS, American journal of medical genetics, 58(1), 1995, pp. 13-17
MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS
Authors: GUIONALMEIDA ML RODINI ESO
Citation: Ml. Guionalmeida et Eso. Rodini, MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS, American journal of medical genetics, 57(3), 1995, pp. 377-379
NEWLY RECOGNIZED AUTOSOMAL RECESSIVE FACIOTHORACOSKELETAL SYNDROME
Authors: RICHIERICOSTA A GUIONALMEIDA ML LAURIS JRP FERREIRA DM
Citation: A. Richiericosta et al., NEWLY RECOGNIZED AUTOSOMAL RECESSIVE FACIOTHORACOSKELETAL SYNDROME, American journal of medical genetics, 49(2), 1994, pp. 224-228
MENTAL-RETARDATION, STRUCTURAL ANOMALIES OF THE CENTRAL-NERVOUS-SYSTEM, ANOPHTHALMIA AND ABNORMAL NARES - A NEW MCA MR SYNDROME OF UNKNOWN CAUSE/
Authors: RICHIERICOSTA A GUIONALMEIDA ML
Citation: A. Richiericosta et Ml. Guionalmeida, MENTAL-RETARDATION, STRUCTURAL ANOMALIES OF THE CENTRAL-NERVOUS-SYSTEM, ANOPHTHALMIA AND ABNORMAL NARES - A NEW MCA MR SYNDROME OF UNKNOWN CAUSE/, American journal of medical genetics, 47(5), 1993, pp. 702-706
CLEFT PALATE-LATERAL SYNECHIAE SYNDROME - REPORT ON 3 NEW PATIENTS WITH ADDITIONAL FINDINGS AND EVIDENCE FOR VARIABILITY AND HETEROGENEITY
Authors: NAKATA NMK GUIONALMEIDA ML RICHIERICOSTA A
Citation: Nmk. Nakata et al., CLEFT PALATE-LATERAL SYNECHIAE SYNDROME - REPORT ON 3 NEW PATIENTS WITH ADDITIONAL FINDINGS AND EVIDENCE FOR VARIABILITY AND HETEROGENEITY, American journal of medical genetics, 47(3), 1993, pp. 330-332
NEWLY RECOGNIZED AUTOSOMAL RECESSIVE MCA MR OVERGROWTH SYNDROME
Authors: RICHIERICOSTA A GUIONALMEIDA ML COHEN MM
Citation: A. Richiericosta et al., NEWLY RECOGNIZED AUTOSOMAL RECESSIVE MCA MR OVERGROWTH SYNDROME, American journal of medical genetics, 47(2), 1993, pp. 278-280
NEWLY RECOGNIZED BLEPHAROFACIOSKELETAL SYNDROME
Authors: RICHIERICOSTA A GUIONALMEIDA ML RODINI ESO PEREIRA SCS COHEN MM
Citation: A. Richiericosta et al., NEWLY RECOGNIZED BLEPHAROFACIOSKELETAL SYNDROME, American journal of medical genetics, 46(6), 1993, pp. 620-622
MANDIBULOFACIAL DYSOSTOSIS - REPORT ON 2 BRAZILIAN FAMILIES SUGGESTING AUTOSOMAL RECESSIVE INHERITANCE
Authors: RICHIERICOSTA A BORTOLOZO MA LAURIS JRP LAURIS RCMC GUIONALMEIDA ML MARQUES D MORETI D
Citation: A. Richiericosta et al., MANDIBULOFACIAL DYSOSTOSIS - REPORT ON 2 BRAZILIAN FAMILIES SUGGESTING AUTOSOMAL RECESSIVE INHERITANCE, American journal of medical genetics, 46(6), 1993, pp. 659-664
Risultati: 1-18 |