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Birth Defects: Original Article Series
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publication venue for
Cytogenetic and clinical notes on a girl with a 46,X,i(Yq) karyotype, H-Y antigen-negative, and a gonadoblastoma
. 14:97-107.
1978
Syndromes of camptodactyly, multiple ankylosis, facial anomalies, and pulmonary hypoplasia
. 14:243-251.
1978
Abnormalities of the mullerian and wolffian duct systems
. 14:37-55.
1978
A previously unrecognized X linked syndrome of dysmorphia
. 11:18-24.
1975
Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation
. 11:380-383.
1975
Familial inguinal hernia affecting females
. 10:332.
1974
Short limbed dwarfism
. 10:261-264.
1974
Two sibs with bilateral renal agenesis
. 10:169-170.
1974
Abnormalities of human autosomes. I. Ambigous genitalia associated with a translocation 46,XY, t(Cq+;Cq-).
. 7:145-149.
1971
Bilateral anorchia: discordance in monozygotic twins.
. 7:196-200.
1971
Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data.
. 7:215-228.
1971
Progressive idiopathic clitoral hypertrophy in a child: a previously undescribed type of female pseudohermaphroditism.
. 7:201-203.
1971
Pseudovaginal perineoscrotal hypospadias (PPSH) in sibs.
. 7:140-144.
1971
Repeated suboptimal pregnancy outcome.
1981
True hermaphroditism: Etiology and phenotyic considerations
1978
Hereditary aspects of ovarian and testicular neoplasia
1976
The relationship of neoplasia to disorders of abnormal sexual differentiation
1976
Gonadal dysgenesis and abnormalities of the human sex chromosomes: current status of phenotypic karyotypic correlations
1975
A child with facial and skeletal dysmorphia reminiscent of Schwartz syndrome.
1975
A patient with the Larsen syndrome.
1975
Generalized dysmorphia of a similar type in two unrelated babies.
1975
Identifiers
International Standard Serial Number (ISSN)
0547-6844