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Prenatal diagnosis of thalidomide syndrome

Prenatal diagnosis, 1987-05, Vol.7 (4), p.295-298

1987

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X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families

American journal of medical genetics, 2003-09, Vol.122A (1), p.51-55

2003

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Ophthalmological, skeletal, and cardiac abnormalities in sibs born to consanguineous parents: A new syndrome?

American journal of medical genetics, 1992-08, Vol.43 (6), p.946-948

1992

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Normal outcome after a 45,X/46,XX/ 46,X,i(Xq) CVS diagnosis

Prenatal diagnosis, 1990-10, Vol.10 (10), p.689-689

1990

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Fronto-facio-nasal dysostosis - a new autosomal recessive syndrome

American journal of medical genetics, 1981, Vol.10 (4), p.409-412

Gollop, Thomaz R.

1981

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The Tel Hashomer camptodactyly syndrome: Report of a new case and review of the literature

American journal of medical genetics, 1988-02, Vol.29 (2), p.411-417

1988

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Odontoonychodysplasia with alopecia: A new pure ectodermal dysplasia with probable autosomal recessive inheritance

American journal of medical genetics, 1985-01, Vol.20 (1), p.197-202

1985

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A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: Acro-fronto-facio-nasal dysostosis syndrome

American journal of medical genetics, 1985-04, Vol.20 (4), p.631-638

1985

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Prenatal ultrasound diagnosis of diastrophic dysplasia at 16 weeks

American journal of medical genetics, 1987-06, Vol.27 (2), p.321-324

1987

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Frontofacionasal dysplasia: Evidence for autosomal recessive inheritance

American journal of medical genetics, 1984-10, Vol.19 (2), p.301-305

1984

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Apparent bifurcatio of distal humerous with oligoectro-syndactyly

American journal of medical genetics, 1983-03, Vol.14 (3), p.591-593

1983

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Familial occurrence of bifid femur and monodactylous ectrodactyly

American journal of medical genetics, 1980, Vol.7 (3), p.319-322

1980

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Blastocyst transfer after embryo biopsy and gender selection in a woman with fragile X premutation and diminished ovarian reserve

JBRA assisted reproduction, 2000, Vol.4 (2)

2000

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Prader-Willi habitus, osteopenia, and camptodactyly (Urban-Rogers-Meyer syndrome): A probable second report

American journal of medical genetics, 1988-12, Vol.31 (4), p.787-792

1988

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The Greig cephalopolysyndactyly syndrome: Report of a family and review of the literature

American journal of medical genetics, 1985-09, Vol.22 (1), p.59-68

1985

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The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family

American journal of medical genetics, 1984-02, Vol.17 (2), p.399-406

1984

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Prenatal diagnosis of 48,XYY, + 21 ascertained through ultrasound anomalies

American journal of medical genetics, 1991-04, Vol.39 (1), p.76-77

1991

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Colpocleisis surgery in the treatment of pelvic organ prolapse in elderly women

MOJ Gerontology & Geriatrics, 2019-11, Vol.4 (6)

2019

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H-Y antigen generating and receptor systems in abnormal sexual development

American journal of medical genetics, 1982-12, Vol.13 (4), p.401-411

1982

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Brief clinical report: distal arthrogryposis type II D in three generations of a Brazilian family

American journal of medical genetics, 1987, Vol.26 (3), p.613-619

1987

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Autosomal recessive anophthalmia with multiple congenital abnormalities-type Waardenburg

American journal of medical genetics, 1983-04, Vol.14 (4), p.607-615

1983

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Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a brazilian family

American journal of medical genetics, 1983-02, Vol.14 (2), p.225-229

1983

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A case of prenatal diagnosis of fetal hydantoin syndrome by ultrasound

Genetics and molecular biology, 1999-06, Vol.22 (2), p.147-150

1999

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Fronto-facio-nasal dysostosis - a new autosomal recessive syndrome

American journal of medical genetics, 1981, Vol.10 (4), p.409-412

Gollop, T R

1981

Volltextzugriff (PDF)

Apparent bifurcatio of distal humerous with oligoectro-syndactyly

American journal of medical genetics, 1983, Vol.14 (3), p.591-593

1983

Volltextzugriff (PDF)

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Prenatal diagnosis of thalidomide syndrome

X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families

Ophthalmological, skeletal, and cardiac abnormalities in sibs born to consanguineous parents: A new syndrome?

Normal outcome after a 45,X/46,XX/ 46,X,i(Xq) CVS diagnosis

Fronto-facio-nasal dysostosis - a new autosomal recessive syndrome

The Tel Hashomer camptodactyly syndrome: Report of a new case and review of the literature

Odontoonychodysplasia with alopecia: A new pure ectodermal dysplasia with probable autosomal recessive inheritance

A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: Acro-fronto-facio-nasal dysostosis syndrome

Prenatal ultrasound diagnosis of diastrophic dysplasia at 16 weeks

Frontofacionasal dysplasia: Evidence for autosomal recessive inheritance

Apparent bifurcatio of distal humerous with oligoectro-syndactyly

Familial occurrence of bifid femur and monodactylous ectrodactyly

Blastocyst transfer after embryo biopsy and gender selection in a woman with fragile X premutation and diminished ovarian reserve

Prader-Willi habitus, osteopenia, and camptodactyly (Urban-Rogers-Meyer syndrome): A probable second report

The Greig cephalopolysyndactyly syndrome: Report of a family and review of the literature

The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family

Prenatal diagnosis of 48,XYY, + 21 ascertained through ultrasound anomalies

Colpocleisis surgery in the treatment of pelvic organ prolapse in elderly women

H-Y antigen generating and receptor systems in abnormal sexual development

Brief clinical report: distal arthrogryposis type II D in three generations of a Brazilian family

Autosomal recessive anophthalmia with multiple congenital abnormalities-type Waardenburg

Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a brazilian family

A case of prenatal diagnosis of fetal hydantoin syndrome by ultrasound

Fronto-facio-nasal dysostosis - a new autosomal recessive syndrome

Apparent bifurcatio of distal humerous with oligoectro-syndactyly

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