ACHEIROPODIA IN JUNQUEIRO SONNET.FROTA PESSOA O.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 10; NO 4; PP. 407-408; BIBL. 4 REF.Article

RECURRENCE RISKS FOR DOWN SYNDROMELISTER TJ; FROTA PESSOA O.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 2; PP. 203-208; BIBL. 14 REF.Article

ATRICHIA, ABNORMAL EEG, EPILEPSY AND MENTAL RETARDATION IN TWO SISTERSRICHIERI COSTA A; FROTA PESSOA O.1979; HUM. HERED.; CHE; DA. 1979; VOL. 29; NO 5; PP. 293-297; BIBL. 17 REF.Article

RISKS OF MANIFESTATION OF HUNTINGTON CHOREA.MARTELLO N; SANTOS JLF; FROTA PESSOA O et al.1978; J. GENET. HUM.; SUISSE; DA. 1978; VOL. 26; NO 1; PP. 33-53; ABS. FR. ALLEM.; BIBL. 19 REF.Article

STRUCTURAL HETEROZYGOSITY IN PARTHENOGENETIC POPULATIONS OF CNEMIDOPHORUS LEMNISCATUS (SAURIA, TEIIDAE) FROM THE AMAZONAS VALLEY = HETEROZYGOTIE STRUCTURALE DANS LES POPULATIONS PARTHENOGENETIQUES DE C. L. (SAURIEN, TEIIDAE) DES VALLEES AMAZONIENNESPECCINI SEALE D; FROTA PESSOA O.1974; CHROMOSOMA; ALLEM.; DA. 1974; VOL. 47; NO 4; PP. 439-451; BIBL. 2P.Article

A TECHNIQUE FOR EVALUATING THE REACTIVITY OF HUMAN SMALL LYMPHOCYTES IN CULTUREMOREIRA FILHO CA; FROTA PESSOA O.1975; CI. E CULT.; BRAS.; DA. 1975; VOL. 27; NO 11; PP. 1234-1236; ABS. PORT.; BIBL. 4 REF.Article

Living history-biography : A rambling rationalistFROTA-PESSOA, O.American journal of medical genetics. 1996, Vol 63, Num 4, pp 585-602, issn 0148-7299Article

USE OF NORMAL DAUGHTER'S CPK LEVELS IN THE ESTIMATION OF HETEROZYGOSITY RISKS IN X-LINKED MUSCULAR DYSTROPHIES = UTILISATION DES NIVEAUX DE CPK DES FILLES SAINES DE CONSULTANTES DANS L'ESTIMATION DES RISQUES D'HETEROZYGOTIE DANS LES DYSTROPHIES MUSCULAIRES LIEES A XZATZ M; FROTA PESSOA O; PERES CA et al.1975; HUM. HERED.; SWITZ.; DA. 1975; VOL. 25; NO 5; PP. 354-359; BIBL. 13 REF.Article

CYTOGENETIC STUDIES ON BRAZILIAN RODENTS.YONENAGA Y; FROTA PESSOA O; KASAHARA S et al.1976; CI. E CULT.; BRAS.; DA. 1976; VOL. 28; NO 2; PP. 202-211; ABS. PORT.; BIBL. 2 P.Article

TURNER'S SYNDROME AND 46,X,I(YQ) KARYOTYPE = SYNDROME DE TURNER ET CARYOTYPE 46,X,I(YQ)MAGNELLI NC; VIANNA MORGANTE AM; FROTA PESSOA O et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 403-406; BIBL. 5REF.Article

THE VARIATION OF RECURRENCE RISKS WITH PENETRANCE FOR ISOLATED CASES OF AUTOSOMAL DOMINANT CONDITIONS.FROTA PESSOA O; OTTO PA; ALIVARES PLAZA JR et al.1976; J. HERED.; U.S.A.; DA. 1976; VOL. 67; NO 4; PP. 256; BIBL. 3 REF.Article

A SEARCH ON KARYOTYPIC MOSAICISM IN MONGOLOID PATIENTS AND THEIR PARENTS.KASAHARA S; VIEGAS PEQUIGNOT EM; FROTA PESSOA O et al.1977; REV. BRAS. PESQ. MED. BIOL.; BRAS.; DA. 1977; VOL. 10; NO 4; PP. 225-235; ABS. PORT.; BIBL. 2 P. 1/2Article

CREATINE-PHOSPHOKINASE (CPK) ACTIVITY IN RELATIVES OF PATIENTS WITH X-LINKED MUSCULAR DYSTROPHIES: A BRAZILIAN STUDY.ZATZ M; FROTA PESSOA O; LEVY JA et al.1976; J. GENET. HUM.; SUISSE; DA. 1976; VOL. 24; NO 2; PP. 153-168; ABS. FR. ALLEM.; BIBL. 2 P. 1/2Article

DOENCA DE NORRIE: DESCRICAO DE UMA FAMILIA COM ACHADOS INCOMUNS = MALADIE DE NORRIE: DESCRIPTION D'UNE FAMILLE AVEC ATTEINTES INHABITUELLES ASSOCIEESNEUSTEIN I; MOREIRA CA FILHO; FROTA PESSOA O et al.1980; ARQ. BRAS. OFTALMOL.; ISSN 0004-2749; BRA; DA. 1980; VOL. 43; NO 3; PP. 100-102; ABS. ENG; BIBL. 9 REF.Article

GENETIC CAUSES OF BLINDNESS IN BRAZILIAN SCHOOL CHILDREN. = CAUSES GENETIQUES DE LA CECITE CHEZ LES ENFANTS BRESILIENS D'AGE SCOLAIRESERRANO CR; NEUSTEIN I; TABOADA LOPES G et al.1978; ARQU. BRAS. OFTALMOL.; BRAS.; DA. 1978; VOL. 41; NO 1; PP. 11-15; ABS. PORT.; BIBL. 15 REF.Article

THE HUMAN Y CHROMOSOME: ITS ROUTINE IDENTIFICATION AND VARIABILITY.BOROVIK CL; LOGHIN GROSSO NS; FROTA PESSOA O et al.1977; REV. BRAS. PESQ. MED. BIOL.; BRAS.; DA. 1977; VOL. 10; NO 3; PP. 159-173; ABS. PORT; BIBL. 21 REF.Article

H-Y ANTIGEN GENERATING AND RECEPTOR SYSTEMS IN ABNORMAL SEXUAL DEVELOPMENTMOREIRA FILHO CA; FROTA PESSOA O; VIANNA MORGANTE AM et al.1982; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 4; PP. 401-411; BIBL. 2 P.Article

AUTOSOMAL DOMINANT LATE ADULT SPINAL MUSCULAR ATROPHY, TYPE FINKELRICHIERI COSTA A; ROGATKO A; LEVISKY R et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 2; PP. 119-128; BIBL. 16 REF.Article

H-Y ANTIGEN IN SWYER SYNDROME AND THE GENETICS OF XY GONADAL DYSGENESISMOREIRA FILHO CA; TOLEDO SPA; BAGNOLLI VR et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 53; NO 1; PP. 51-56; BIBL. 26 REF.Article

CLINICAL SYMPTONS IN A FEMALE CARRIER OF DUCHENNE MUSCULAR DYSTROPHYZATZ M; LEVISKY RB; LEVY JA et al.1973; J. GENET. HUM.; SUISSE; DA. 1973; VOL. 21; NO 4; PP. 297-305; ABS. FR. ALLEM.; BIBL. 13REF.Article

H-Y ANTIGEN EXPRESSION IN A CASE OF XX TRUE HERMAPHRODISMMOREIRA FILHO CA; OTTO PG; MUSTACCHI Z et al.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 55; NO 3; PP. 309-314; BIBL. 20 REF.Article

MYOTONIC DYSTROPHY, SYRINGOMYELIA, AND 2/13 TRANSLOCATION IN THE SAME FAMILY.LEVISKY RB; VIANNA MORGANTE AM; FROTA PESSOA O et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 1; PP. 51-53; BIBL. 15 REF.Article

NEW LINKAGE DATA FOR THE X-LINKED TYPES OF MUSCULAR DYSTROPHY AND G6PD VARIANTS, COLOUR BLINDNESS, AND XG BLOOD GROUPS = NOUVELLES DONNEES SUR LES LIAISONS ENTRE LES TYPES LIES A L'X DE LA DYSTROPHIE MUSCULAIRE ET LES VARIANTES DE LA G6PD, LE DALTONISME ET LES GROUPES SANGUINS XGZATZ M; ITSKAN SB; SANGER R et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 321-327; BIBL. 20REF.Article

A Bayesian method for the estimation of penetrance: application to mandibulofacial and frontonasal dysostosesROGATKO, A; PEREIRA, C. A. B; FROTA-PESSOA, O et al.American journal of medical genetics. 1986, Vol 24, Num 2, pp 231-246, issn 0148-7299Article

Snyder's ratios with incomplete penetranceOTTO, P. A; FROTA-PESSOA, O; POLCAN, S. P et al.The journal of heredity. 1994, Vol 85, Num 4, pp 331-335, issn 0022-1503Article