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New perspectives on the face in fetal alcohol syndrome: What anthropometry tells us

American journal of medical genetics, 2002-05, Vol.109 (4), p.249-260

2002

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Athabascan brainstem dysgenesis syndrome

American journal of medical genetics, 2003-07, Vol.120A (2), p.169-173

2003

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Splenogonadal fusion‐limb defect “syndrome” and associated malformations

American journal of medical genetics, 2003-08, Vol.120A (4), p.518-522

2003

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Limb deficiency with or without Möbius sequence in seven Brazilian children associated with misoprostol use in the first trimester of pregnancy

American journal of medical genetics, 1993-08, Vol.47 (1), p.59-64

1993

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Craniofacial variability index: A simple measure of normal and abnormal variation in the head and face

American journal of medical genetics, 1998-11, Vol.80 (3), p.232-240

1998

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Pontine hypoplasia in Carey–Fineman–Ziter (CFZ) syndrome

American journal of medical genetics, 2004-06, Vol.127A (3), p.288-290

2004

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Primary immunodeficiency in combination with transverse upper limb defect and anal atresia in a 34‐year‐old patient with Jacobsen syndrome

American journal of medical genetics, 2004-04, Vol.126A (3), p.293-298

2004

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Poland anomaly with foot symbrachydactyly

American journal of medical genetics, 2002-05, Vol.109 (4), p.333-334

2002

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Limb defects and congenital anomalies of the genitalia in an infant with homozygous α-thalassemia

American journal of medical genetics, 1997-01, Vol.68 (2), p.158-161

1997

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Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: A new autosomal recessive MCA/MR syndrome?

American journal of medical genetics, 2001-07, Vol.102 (1), p.63-67

2001

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Association of prenatal vascular disruptions with decreased maternal age

American journal of medical genetics, 1997-03, Vol.69 (3), p.237-239

Lubinsky, Mark S.

1997

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Postnatal growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy

American journal of medical genetics, 2003-01, Vol.116A (2), p.164-169

2003

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Genetic locus on chromosome 6p for multicystic renal dysplasia, pelvi-ureteral junction stenosis, and vesicoureteral reflux

American journal of medical genetics, 1995-11, Vol.59 (3), p.396-397

1995

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Amniotic band sequence and limb defects: Data from a population-based study

American journal of medical genetics, 1993-06, Vol.46 (5), p.497-500

1993

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Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome

American journal of medical genetics, 1991-01, Vol.38 (1), p.69-73

1991

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Poland anomaly with unusual associated anomalies: Case report of an apparent disorganization defect

American journal of medical genetics, 1994-10, Vol.52 (4), p.402-405

1994

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Limb anomalies following chorionic villus sampling: A registry based case-control study

American journal of medical genetics, 1992-12, Vol.44 (6), p.856-864

1992

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Poland sequence with dextrocardia: Which comes first?

American journal of medical genetics, 1997-12, Vol.73 (2), p.194-196

1997

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Terminal transverse limb defects associated with familial cavernous angiomatosis

American journal of medical genetics, 1992-02, Vol.42 (3), p.346-351

1992

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Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face

American journal of medical genetics, 1993-11, Vol.47 (6), p.917-920

Winter, R. M.

1993

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Splenogonadal fusion limb defect syndrome: Report of five new cases and review

American journal of medical genetics, 1999-10, Vol.86 (4), p.347-358

1999

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Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome: An additional clinical observation

American journal of medical genetics, 1992-02, Vol.42 (3), p.398-399

1992

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Congenital microgastria and hypoplastic upper limb anomalies

American journal of medical genetics, 1989-03, Vol.32 (3), p.368-370

1989

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The syndrome of Möbius sequence, peripheral neuropathy, and hypogonadotropic hypogonadism

American journal of medical genetics, 1990-12, Vol.37 (4), p.578-582

1990

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De novo apparently balanced reciprocal translocation between 5q1l.2 and 17q23 associated with Klippel-Feil anomaly and type A1 brachydactyly

American journal of medical genetics, 1995-07, Vol.57 (3), p.447-449

1995

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New perspectives on the face in fetal alcohol syndrome: What anthropometry tells us

Athabascan brainstem dysgenesis syndrome

Splenogonadal fusion‐limb defect “syndrome” and associated malformations

Limb deficiency with or without Möbius sequence in seven Brazilian children associated with misoprostol use in the first trimester of pregnancy

Craniofacial variability index: A simple measure of normal and abnormal variation in the head and face

Pontine hypoplasia in Carey–Fineman–Ziter (CFZ) syndrome

Primary immunodeficiency in combination with transverse upper limb defect and anal atresia in a 34‐year‐old patient with Jacobsen syndrome

Poland anomaly with foot symbrachydactyly

Limb defects and congenital anomalies of the genitalia in an infant with homozygous α-thalassemia

Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: A new autosomal recessive MCA/MR syndrome?

Association of prenatal vascular disruptions with decreased maternal age

Postnatal growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy

Genetic locus on chromosome 6p for multicystic renal dysplasia, pelvi-ureteral junction stenosis, and vesicoureteral reflux

Amniotic band sequence and limb defects: Data from a population-based study

Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome

Poland anomaly with unusual associated anomalies: Case report of an apparent disorganization defect

Limb anomalies following chorionic villus sampling: A registry based case-control study

Poland sequence with dextrocardia: Which comes first?

Terminal transverse limb defects associated with familial cavernous angiomatosis

Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face

Splenogonadal fusion limb defect syndrome: Report of five new cases and review

Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome: An additional clinical observation

Congenital microgastria and hypoplastic upper limb anomalies

The syndrome of Möbius sequence, peripheral neuropathy, and hypogonadotropic hypogonadism

De novo apparently balanced reciprocal translocation between 5q1l.2 and 17q23 associated with Klippel-Feil anomaly and type A1 brachydactyly

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