(Q39505161)

12 September 2017

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title

Developmental genetics. (English)

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12 September 2017

C J Epstein

1

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12 September 2017

publication date

1 October 1986

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12 September 2017

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12 September 2017

volume

42

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12 September 2017

issue

10

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12 September 2017

page(s)

1117-1128

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Evaluation and re-evaluation of genetic radiation hazards in man. III. Other relevant data and risk assessment

12 September 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01941286

Synthesis of Interferon-Induced Polypeptides in Normal and Chromosome 21-Aneuploid Human Fibroblasts: Relationship to Relative Sensitivities in Antiviral Assays

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01941286

A cytogenetic study of spontaneous abortions in Hawaii

21 January 2018

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12 December 2020

Genetic disorders of collagen metabolism.

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12 December 2020

Comparative gene mapping of human chromosome 21 and mouse chromosome 16

1 reference

12 December 2020

Analysis of two-dimensional protein patterns from mouse embryos with different trisomies

1 reference

12 December 2020

In vivo and in vitro studies on the early embryonic lethal oligosyndactylism (Os) in the mouse

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12 December 2020

The development of monosomy 19 mouse embryos

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12 December 2020

Studies on syndrome of diabetes insipidus associated with oligosyndactyly in mice

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12 December 2020

Value of an animal model for trisomy

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12 December 2020

Trisomy 16 in the mouse fetus associated with generalized edema and cardiovascular and urinary tract anomalies.

1 reference

12 December 2020

Down syndrome—a disruption of homeostasis

1 reference

12 December 2020

Abnormalities of the in vitro cellular and humoral responses to tetanus and influenza antigens with concomitant numerical alterations in lymphocyte subsets in Down syndrome (trisomy 21)

1 reference

12 December 2020

Genetic, metabolic, and biochemical aspects of the porphyrias.

1 reference

12 December 2020

Changes in plasma membrane proteins and glycoproteins during normal and brachypod mouse limb development

1 reference

12 December 2020

The murine Ah locus: in utero toxicity and teratogenesis associated with genetic differences in benzo[a]pyrene metabolism

1 reference

12 December 2020

The chondro-osseous dysplasia of adenosine deaminase deficiency with severe combined immunodeficiency

1 reference

12 December 2020

Type I osteogenesis imperfecta: a nonfunctional allele for pro alpha 1 (I) chains of type I procollagen

1 reference

12 December 2020

The elements of the bithorax complex

1 reference

12 December 2020

T-lymphocyte function and sensitivity to interferon in trisomy 21

1 reference

12 December 2020

Clinical and genetic aspects of antithrombin III deficiency

1 reference

12 December 2020

Errors of morphogenesis: concepts and terms. Recommendations of an international working group.

1 reference

12 December 2020

Embryonic to adult conversion of neural cell adhesion molecules in normal and staggerer mice

1 reference

12 December 2020

Medical genetics. Collagen and inherited connective tissue diseases

1 reference

12 December 2020

Stem cell deficiencies and thymic abnormalities in fetal mouse trisomy 16.

1 reference

12 December 2020

Direct evidence that the gene product of the human chromosome 21 locus, IFRC, is the interferon-α receptor

1 reference

12 December 2020

Mechanisms of Cortical Development: A View From Mutations in Mice

1 reference

12 December 2020

Chromosome examination of newborn children: purpose and ethical aspects

1 reference

12 December 2020

Genes coding for sensitivity to interferon (IfRec) and soluble superoxide dismutase (SOD-1) are linked in mouse and man and map to mouse chromosome 16

1 reference

12 December 2020

Marfan syndrome: abnormal alpha 2 chain in type I collagen

1 reference

12 December 2020

Genetics of Drosophila embryogenesis

1 reference

12 December 2020

Trisomy in the fetal backcross progeny of male and female metacentric heterozygotes of the mouse. i

1 reference

12 December 2020

Dosage effects for superoxide dismutase-1 in nucleated cells aneuploid for chromosome 21

1 reference

12 December 2020

Abnormal plasminogen. A hereditary molecular abnormality found in a patient with recurrent thrombosis

1 reference

12 December 2020

Preimplantation lethality of monosomy for mouse chromosome 19

1 reference

12 December 2020

Production of viable adult trisomy 17 reversible diploid mouse chimeras

1 reference

12 December 2020

Peroxisomal organization in normal and cerebrohepatorenal (Zellweger) syndrome fibroblasts

1 reference

12 December 2020

Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis

1 reference

12 December 2020

Interferon induction of (2??5?) oligoisoadenylate synthetase in diploid and trisomy 21 human fibroblasts: Relation to dosage of the interferon receptor gene (IRFC)

1 reference

12 December 2020

A compendium of the genetically induced congenital malformations of the house mouse

1 reference

12 December 2020

Gout with superactive phosphoribosylpyrophosphate synthetase due to increased enzyme catalytic rate

1 reference

12 December 2020

The multifactorial/threshold concept -- uses and misuses.

1 reference

12 December 2020

The Marfan Syndrome: A Deficiency in Chemically Stable Collagen Cross-Links

1 reference

12 December 2020

Combined immunodeficiency disease associated with adenosine deaminase deficiency. Report on a workshop held in Albany, New York, October 1, 1973

1 reference

12 December 2020

Mouse trisomy 16: an animal model of human trisomy 21 (Down syndrome)

1 reference

12 December 2020

Genetics of cortisone-induced cleft palate in the mouse-embryonic and maternal effects

1 reference

12 December 2020

The analysis of cell differentiation by hybridization of somatic cells

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12 December 2020

The developmental field concept in clinical genetics.

1 reference

12 December 2020

Diminished type I collagen synthesis and reduced alpha 1(I) collagen messenger RNA in cultured fibroblasts from patients with dominantly inherited (type I) osteogenesis imperfecta

1 reference

12 December 2020

Mutant mouse tottering: selective increase of locus ceruleus axons in a defined single-locus mutation

1 reference

12 December 2020

Oligosyndactyly: a lethal mutation in the mouse that results in mitotic arrest very early in development

1 reference

12 December 2020

Glutaric acidemia type II: a form with deleterious intrauterine effects

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12 December 2020

The mutation rate in man

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12 December 2020

Genetic predisposition to phenytoin-induced birth defects

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12 December 2020

Expression during embryogenesis of a mouse gene with sequence homology to the Drosophila engrailed gene

1 reference

12 December 2020

The molecular organization of the Antennapedia locus of Drosophila

1 reference

12 December 2020

Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): Production of viable trisomy 16 ↔ diploid mouse chimeras

1 reference

12 December 2020

The early lethality of autosomal monosomy in the mouse.

1 reference

12 December 2020

Genetic control of very early mammalian development

1 reference

12 December 2020

Systematic approach to the study of trisomy in the mouse. II

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12 December 2020

The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects

1 reference

12 December 2020

Clinicopathologic conference: a three-month-old infant with failure to thrive, hepatomegaly, and neurological impairment

1 reference

12 December 2020

Familial hypercholesterolemia. A genetic regulatory defect in cholesterol metabolism

1 reference

12 December 2020

Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).

1 reference

12 December 2020

Report of the Committee on Comparative Mapping

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12 December 2020

Neuronal differentiation in cultures of weaver (wv) mutant mouse cerebellum

1 reference

12 December 2020

Cytoplasmic activation of human nuclear genes in stable heterocaryons

1 reference

12 December 2020

Gene dosage effect for glycinamide ribonucleotide synthetase in human fibroblasts trisomic for chromosome 21

1 reference

12 December 2020

Abnormal proteodermatan sulfate in three patients with Coffin-Lowry syndrome

1 reference

12 December 2020

Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions

1 reference

12 December 2020

Oligosyndactylism, an early embryonic lethal in the mouse

1 reference

12 December 2020

Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability

1 reference

12 December 2020

The effect of trisomy 21 on the patterns of polypeptide synthesis in human fibroblasts

1 reference

12 December 2020

Two homoeo box loci mapped in evolutionarily related mouse and human chromosomes

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12 December 2020

Comparative chromosome mapping of a conserved homoeo box region in mouse and human

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12 December 2020

Identifiers

DOI

10.1007/BF01941286

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12 September 2017

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